Alkoxy pyrazoles as soluble guanylate cyclase activators

ABSTRACT

The present invention relates to compounds of formula (I): 
                         
and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6  and R 7  are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.

FIELD OF THE INVENTION

This invention relates to heterocyclic compounds which are useful asactivators of soluble guanylate cyclase and are thus useful for treatinga variety of diseases that are mediated or sustained by decreased ordiminished soluble guanylate cyclase activity, including cardiovasculardiseases, renal disease, diabetes, fibrotic disorders, urologicdisorders, neurological disorders and inflammatory disorders. Thisinvention also relates to pharmaceutical compositions comprising thesecompounds, methods of using these compounds in the treatment of variousdiseases and disorders, processes for preparing these compounds andintermediates useful in these processes.

BACKGROUND

Soluble guanylate cyclase (sGC) is a receptor for nitric oxide (NO)which is found in the cytoplasm of many cell types. In humans,functional sGC is a heterodimer composed of either an alpha 1 or alpha 2subunit combined with the beta 1 subunit which has a heme prostheticgroup. Under non-pathophysiological conditions, NO binding to the hemeof sGC activates the enzyme to catalyze the conversion ofguanosine-5′-triphosphate (GTP) to cyclic guanosine monophosphate(cGMP). cGMP is a second messenger which exerts effects by modulatingcGMP dependent protein kinase (PKG) isoforms, phosphodiesterases, andcGMP gated ion channels. In doing so, sGC has been demonstrated tomodulate numerous pathways associated with diseases including arterialhypertension, pulmonary hypertension, atherosclerosis, heart failure,liver cirrhosis, renal fibrosis, and erectile dysfunction (O. Evgenov etal., Nature Reviews, 2006, 5, 755-768 and Y. Wang-Rosenke et al., Curr.Med. Chem., 2008, 15, 1396-1406).

Under normal conditions, the iron in sGC exists in the ferrous statewhich is capable of binding to NO and carbon monoxide (CO). However,under conditions of oxidative stress which can occur in variousdiseases, published reports indicate that the heme iron becomes oxidizedto the ferric state which is incapable of being activated by NO or CO.The inability of NO to signal through sGC with an oxidized heme iron hasbeen hypothesized to contribute to disease processes. Recently, twonovel classes of compounds have been described which potentiate sGCactivity in a heme dependent (sGC stimulators) and heme independent (sGCactivators) manner. The activity of sGC stimulators synergizes with NOto increase cGMP production while sGC activators are only additive withNO to augment cGMP levels (O. Evgenov et al., Nature Reviews, 2006, 5,755-768). Both stimulators and activators of sGC have demonstratedbenefit in animal models of disease. Activators of sGC provide theadvantage of being able to preferentially target the diseased,non-functional form of the enzyme. sGC activators include BAY 58-2667(cinaciguat) (J-P Stasch et al., Brit J. Pharmacol., 2002, 136, 773-783)and HMR-1766 (ataciguat) (U. Schindler et al., 2006, Mol. Pharmacol.,69, 1260-1268).

NO has an important role in maintaining normal cellular and tissuefunction. However, adequate signaling in the NO pathway can be disruptedat a number of steps. NO signaling can be impaired by reduced levels ofnitric oxide synthase (NOS) enzymes, NOS activity, NO bioavailability,sGC levels, and sGC activity. sGC activators have the potential tobypass the functional impediment produced by all of these impairments.Since sGC activation occurs downstream of NO synthesis or NOavailability, these deficiencies will not impact the activity of sGCactivators. As described above, the activity of sGC in which function isdisrupted by heme iron oxidation will be corrected by sGC activators.Thus, sGC activators have the potential to provide benefit in manydiseases caused by defective signaling in the NO pathway.

Activation of sGC has the potential to provide therapeutic benefit foratherosclerosis and arteriosclerosis. Cinaciguat treatment has beendemonstrated to prevent neointimal hyperplasia after endothelialdenudation by wire injury of the carotid artery in rats (K. Hirschberget al., Cardiovasc. Res., 2010, 87, Suppl. 1, 5100, Abstract 343).Ataciguat inhibited atherosclerotic plaque formation in ApoE−/− micefeed a high fat diet (M. van Eickels, BMC Pharmacology, 2007, 7, Suppl.1, S4). Decreased NO production in endothelial nitric oxide synthase(eNOS) deficient mice increased vascular inflammation and insulinresistance in response to nutrient excess. In the same study, thephosphodiesterase 5 (PDE5) inhibitor sildenafil reduced vascularinflammation and insulin resistance in mice fed a high-fat diet (N.Rizzo et al., Arterioscler. Thromb. Vasc. Biol., 2010, 30, 758-765).Lastly, after balloon-injury of rat carotid arteries in vivo, a sGCstimulator (YC-1) inhibited neotima formation (C. Wu, J. Pharmacol.Sci., 2004, 94, 252-260

The complications of diabetes may be reduced by sGC activation. Glucoseinduced suppression of glucagon release is lost in pancreatic isletsthat lack PKG, thus suggesting a role of sGC mediated cGMP production inglucose regulation (V. Leiss et al., BMC Pharmacology, 2009, 9, Suppl.1, P40).

It is well established clinically that elevation of cGMP by treatmentwith PDE5 inhibitors is efficacious for the treatment of erectiledysfunction (ED). However, 30% of ED patients are resistant to PDE5inhibitor treatment (S. Gur et al., Curr. Pharm. Des., 2010, 16,1619-1633). The sGC stimulator BAY-41-2272 is able to relax corpuscavernosum muscle in a sGC dependent manner, thus suggesting thatincreased sGC activity could provide benefit in ED patients (C. Teixeiraet al., J. Pharmacol. & Exp. Ther., 2007, 322, 1093-1102). Furthermore,sGC stimulators and sGC activators used individually or either incombination with PDE5 inhibitor was able to treat ED in animal models(WO 10/081,647).

There is evidence that sGC activation may be useful in preventing tissuefibrosis, including that of the lung, liver, and kidney. The processesof epithelial to mesenchyal transition (EMT) and fibroblast tomyofibroblast conversion are believed to contribute to tissue fibrosis.When either cincaciguat or BAY 41-2272 was combined with sildenafil,lung fibroblast to myofibroblast conversion was inhibited (T. Dunkern etal., Eur. J. Pharm., 2007, 572, 12-22). NO is capable of inhibiting EMTof alveolar epithelial cells (S. Vyas-Read et al., Am. J. Physiol. LungCell Mol. Physiol., 2007, 293, 1212-1221), suggesting that sGCactivation is involved in this process. NO has also been shown toinhibit glomerular TGF beta signaling (E. Dreieicher et al., J. Am. Soc.Nephrol., 2009, 20, 1963-1974) which indicates that sGC activation maybe able to inhibit glomerular sclerosis. In a pig serum model and carbontetrachloride model of liver fibrosis, an sGC activator (BAY 60-2260)was effective at inhibiting fibrosis (A. Knorr et al.,Arzneimittel-Forschung, 2008, 58, 71-80).

Clinical studies have demonstrated efficacy using the sGC activatorcinaciguat for the treatment of acute decompensated heart failure (H.Lapp et al., Circulation, 2009, 119, 2781-2788). This is consistent withresults from a canine tachypacing-induced heart failure model in whichacute intravenous infusion of cinaciguat was able to produce cardiacunloading (G. Boerrigter et al., Hypertension, 2007, 49, 1128-1133). Ina rat myocardial infarction induced chronic heart failure model, HMR1766 improved cardiac function and reduced cardiac fibrosis which wasfurther potentiated by ramipril (F. Daniela, Circulation, 2009, 120,Suppl. 2, S852-S853).

Activators of sGC can be used to treat hypertension. This has beenclearly demonstrated in clinical studies in which the dose of cinaciguatis titrated based on the magnitude of blood pressure reduction achieved(H. Lapp et al., Circulation, 2009, 119, 2781-2788). Preclinical studiesusing cinaciguat had previously shown the ability of sGC activation toreduce blood pressure (J.-P. Stasch et al., 2006, J. Clin. Invest., 116,2552-2561). Similar findings have been reported using the sGC activatorHMR 1766 as well (U. Schindler et al., 2006, Mol. Pharmacol., 69,1260-1268).

The activation of sGC has the potential to reduce inflammation byeffects on the endothelium. BAY 41-2272 and a NO donor inhibitedleukocyte rolling and adhesion in eNOS deficient mice. This wasdemonstrated to be mediated by down-regulation of expression of theadhesion molecule P-selectin (A. Ahluwalla et al., Proc. Natl. Acad.Sci. USA, 2004, 101, 1386-1391). Inhibitors of NOS and sGC were shown toincrease endotoxin (LPS) induced ICAM expression on mesentericmicrocirculation vessels. This was reduced by an NO donor in a cGMPdependent manner. Treatment of mice with NOS or sGC inhibitors increasedneutrophil migration, rolling, and adhesion induced by LPS orcarrageenen (D. Dal Secco, Nitric Oxide, 2006, 15, 77-86). Activation ofsGC has been shown to produce protection from ischemia-reperfusioninjury using BAY 58-2667 in both in vivo and in an isolated heart model(T. Krieg et al., Eur. Heart J., 2009, 30, 1607-6013). Similar resultswere obtained using the same compound in a canine model of cardioplegicarrest and extracorporeal circulation (T. Radovits et al., Eur J.Cardiothorac. Surg., 2010).

Some studies have indicated the potential of sGC activation to haveantinociceptive effects. In streptozotocin-induced diabetes models ofnociception in mice (writhing assay) and rats (paw hyperalgesia),elevation of cGMP levels by administration of sildenafil blocked thepain response, which in turn was abrogated by a NOS or sGC inhibitor (C.Patil et al., Pharm., 2004, 72, 190-195). The sGC inhibitor1H-1,2,4.-oxadiazolo-4,2-a.quinoxalin-1-one (ODQ) has been demonstratedto block the antinociceptive effects of various agents includingmeloxicam and diphenyl diselenide in a formalin induced pain model (P.Aguirre-Banuelos et al., Eur. J. Pharmacol., 2000, 395, 9-13 and L.Savegnago et al., J. Pharmacy Pharmacol., 2008, 60, 1679-1686) andxylazine in a paw pressure model (T. Romero et al., Eur. J. Pharmacol.,2009, 613, 64-67). Furthermore, ataciguat was antinociceptive in thecarrageenan model of inflammatory triggered thermal hyperalgesia and thespared nerve injury model of neuropathic pain in mice (WO 09/043,495).

Inhibition of PDE9, a phosphodiesterase specific for cGMP expressed inthe brain, has been shown to improve long-term potentiation (F. van derStaay et al., Neuropharmacol. 2008, 55, 908-918). In the central nervoussystem, sGC is the primary enzyme which catalyzes the formation of cGMP(K. Domek-Lopacinska et al., Mol. Neurobiol., 2010, 41, 129-137). Thus,sGC activation may be beneficial in treating Alzheimer's and Parkinson'sdisease. In a phase II clinical study, the sGC stimulator riociguat, wasefficacious in treating chronic thromboembolic pulmonary hypertensionand pulmonary arterial hypertension (H. Ghofrani et al., Eur. Respir.J., 2010, 36, 792-799). These findings extend the preclinical studies inwhich BAY 41-2272 and cinaciguat reduced pulmonary hypertension in mouse(R. Dumitrascu et al., Circulation, 2006, 113, 286-295) and lamb (O.Evgenov et al., 2007, Am. J. Respir. Crit. Care Med., 176, 1138-1145)models. Similar results were obtained using HMR 1766 in a mouse model ofpulmonary hypertension (N. Weissmann et al., 2009, Am. J. Physiol. LungCell. Mol. Physiol., 297, L658-665).

Activation of sGC has the potential to treat chronic kidney disease.Both BAY 58-2667 and HMR 1766 improved renal function and structure in arat subtotal nephrectomy model of kidney disease (P. Kalk et al., 2006,Brit. J. Pharmacol., 148, 853-859 and K. Benz et al., 2007, Kidney BloodPress. Res., 30, 224-233). Improved kidney function and survival wasprovided by BAY 58-2667 treatment in hypertensive renin transgenic rats(TG(mRen2)27 rats) treated with a NOS inhibitor (J.-P. Stasch et al.,2006, J. Clin. Invest., 116, 2552-2561). BAY 41-2272 treatment preservedkidney function and structure in a chronic model of kidney disease inrats induced by uninephrectomy and anti-thyl antibody treatment (Y. Wanget al., 2005, Kidney Intl., 68, 47-61). Diseases caused by excessiveblood clotting may be treated with sGC activators. Activation of sGCusing BAY 58-2667 was capable of inhibiting platelet aggregation inducedby various stimuli ex vivo. Additionally, this compound inhibitedthrombus formation in vivo in mice and prolonged bleeding time (J.-P.Stasch et al., 2002, Brit. J. Pharmacol., 136, 773-783). In anotherstudy using HMR 1766, in vivo platelet activation was inhibited instreptozotocin treated rats (A. Schafer et al., 2006, Arterioscler.Thromb. Vasc. Biol., 2006, 26, 2813-2818).

sGC activation may also be beneficial in the treatment of urologicdisorders (WO/08138483). This is supported by clinical studies using thePDE5 inhibitor vardenafil (C. Stief et al., 2008, Eur. Urol., 53,1236-1244). The soluble guanylate cyclase stimulator BAY 41-8543 wasable to inhibit prostatic, urethra, and bladder smooth muscle cellproliferation using patient samples (B. Fibbi et al., 2010, J. Sex.Med., 7, 59-69), thus providing further evidence supporting the utilityof treating urologic disorders with sGC activators.

The above studies provide evidence for the use of sGC activators totreat cardiovascular diseases including hypertension, atherosclerosis,peripheral artery disease, restenosis, stroke, heart failure, coronaryvasospasm, cerebral vasospasm, ischemia/reperfusion injury,thromboembolic pulmonary hypertension, pulmonary arterial hypertension,stable and unstable angina, thromboembolic disorders. Additionally, sGCactivators have the potential to treat renal disease, diabetes, fibroticdisorders including those of the liver, kidney and lungs, urologicdisorders including overactive bladder, benign pro static hyperplasia,and erectile dysfunction, and neurological disorders includingAlzheimer's disease, Parkinson's disease, as well as neuropathic pain.Treatment with sGC activators may also provide benefits in inflammatorydisorders such as psoriasis, multiple sclerosis, arthritis, asthma, andchronic obstructive pulmonary disease.

BRIEF SUMMARY OF THE INVENTION

The present invention provides novel compounds which activate orpotentiate sGC and are thus useful for treating a variety of diseasesand disorders that can be alleviated by sGC activation or potentiationincluding cardiovascular, inflammatory and renal diseases. Thisinvention also relates to pharmaceutical compositions comprising thesecompounds, methods of using these compounds in the treatment of variousdiseases and disorders, processes for preparing these compounds andintermediates useful in these processes.

In a further aspect, the present invention provides activators ofsoluble guanylate cyclase having solubility properties consistent withacceptable pharmacokinetic properties. As is known in the art, poorlysoluble compounds may suffer from poor human exposure. The compounds ofthe present invention would be expected to have exposure propertiesconsistent with being a suitable drug.

In a further aspect, the present invention provides compounds withmetabolic stability properties consistent with acceptablepharmacokinetic properties. As is known in the art, compounds havingpoor metabolic stability may not readily achieve desirable therapeuticlevels. The compounds of the present invention would be expected to havemetabolic stability properties consistent with being a suitable drug.

DETAILED DESCRIPTION OF THE INVENTION

In an embodiment, there are provided compounds of the formula I

wherein:A is a 5-7 membered saturated heterocyclyl group containing one nitrogenand optionally one oxygen, wherein one carbon of said heterocyclyl groupis optionally substituted with one or two groups selected from C₁₋₃alkyland oxo;R¹ is C₁₋₄ alkyl optionally substituted with a methoxy group;R² is selected from H, F, Cl, C₁₋₃alkyl, —CN, —OMe and —CF₃;R³ is selected from H and —CH₃;R⁴ is selected from H, F, —CH₃ and —OMe;R⁵ is selected from H, Cl, —CH₃, —CH₂CH₃, —CF₃, F, and —OMe;R⁶ is bonded to the nitrogen on A and is selected from H, C₁₋₆alkyl,—(CH₂)_(n)C₃₋₆cycloalkyl, —C(O)C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl,—(CH₂)_(n) aryl —(CH₂)_(n) heteroaryl, —SO₂aryl, SO₂C₁₋₆alkyl whereinsaid C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl, —(CH₂)_(n) cycloalkyl,—(CH₂)_(n) aryl and —(CH₂)_(n) heteroaryl are optionally substitutedwith one to four groups independently selected from C₁₋₃alkyl, halogen,C₁₋₃alkoxy, —CF₃, —OH, oxo, —(CH₂)₁₋₃O(CH₂)₂₋₃OH, and —SO₂CH₃;R⁷ is selected from H, —CH₃, —CH₂CH₃, —CF₃, F, and —CN;n is 0, 1 or 2or a salt thereof.

In another embodiment, there are provided compounds as described in theembodiment above, wherein:

A is a 5-7 membered saturated heterocyclyl group containing onenitrogen, wherein one carbon of said heterocyclyl group is optionallysubstituted with one or two C₁₋₃alkyl groups;

R¹ is C₁₋₃alkyl;

R² is selected from H, F, Cl, C₁₋₃alkyl, —CN, —OMe and —CF₃;

R³ is selected from H and —CH₃;

R⁴ is selected from H and F;

R⁵ is selected from H, Cl and —CH₃;

R⁶ is bonded to the nitrogen on A and is selected from H, C₁₋₆alkyl,—(CH₂)_(n)C₃₋₆cycloalkyl, —C(O)C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl,—(CH₂)_(n) aryl and —(CH₂)_(n) heteroaryl, wherein said C₁₋₆alkyl,—(CH₂)_(n) heterocyclyl, —(CH₂)_(n) cycloalkyl, —(CH₂)_(n) aryl and—(CH₂)_(n) heteroaryl are optionally substituted with one to four groupsindependently selected from C₁₋₃alkyl, halogen, C₁₋₃alkoxy, —CF₃, —OHand —SO₂CH₃;R⁷ is H;andn is 0, 1 or 2;or a salt thereof.

In another embodiment, there are provided compounds as described in anyof the embodiments above, wherein:

R¹ is methyl, ethyl or isopropyl; and

the group

is selected from:

or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein:

R² is selected from —CH₃, F, Cl, and —CF₃; and

R⁶ is selected from H, C₁₋₆alkyl, —(CH₂)_(n)C₃₋₆cycloalkyl,—C(O)C₁₋₆alkyl and —(CH₂)_(n) heterocyclyl, wherein said C₁₋₆alkyl,—(CH₂)_(n) cycloalkyl and —(CH₂)_(n) heterocyclyl are optionallysubstituted with one to four groups independently selected fromC₁₋₃alkyl, halogen, C₁₋₃alkoxy, —CF₃, —OH and —SO₂CH₃;or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein each heterocyclyl referred to in R⁶ isselected from oxetanyl, tetrahydrofuranyl, tetrahydropyranyl,2-oxabicyclo[3.2.0]heptanyl, [1,4]dioxanyl, 8-oxabicyclo[3.2.1]octanyl,1-oxaspiro[4.5]decanyl and pyrrolidin-2-one;

each heteroaryl referred to in R⁶ is selected from imidazolyl,isoxazolyl, pyrazinyl, pyrazolyl, pyridinyl, pyrimidinyl, thiazolyl and4,5,6,7-tetrahydrobenzothiazolyl;

and each aryl referred to in R⁶ is phenyl;

or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein:

R⁶ is —(CH₂)_(n) heterocyclyl, wherein said heterocyclyl is selectedfrom oxetanyl, tetrahydrofuranyl, tetrahydropyranyl,2-oxabicyclo[3.2.0]heptanyl, [1,4]dioxanyl, 8-oxabicyclo[3.2.1]octanyland 1-oxaspiro[4.5]decanyl;

or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein:

R² is —CH₃;

R³ is H;

R⁴ is H or —CH₃;

R⁵ is H, or —CH₃;

R⁷ is in the position para to R⁵ and is H, —CH₃ or —CH₂CH₃;

or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein:

the group

or a salt thereof.

In another embodiment there are provided compounds as described in anyof the embodiments above, wherein:

R³ is H; and

R⁴ is H;

or a salt thereof.

Table 1 shows representative compounds of the invention which can bemade by the general synthetic schemes, the examples, and known methodsin the art.

TABLE 1 Cpd No. Structure 1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

22

23

24

25

26

27

28

29

30

31

32

33

34

35

36

37

38

39

40

41

42

43

44

45

46

47

48

49

50

51

52

53

54

55

56

57

58

59

60

61

62

63

64

65

66

67

68

69

70

71

72

73

74

75

76

77

78

79

80

81

82

83

84

85

86

87

88

89

90

91

92

93

94

95

96

97

98

99

100

101

102

103

104

105

106

107

108

109

110

111

112

113

114

115

116

117

118

119

120

121

122

123

124

125

126

127

128

129

130

131

132

133

134

135

136

137

138

139

140

141

142

143

144

145

146

147

148

149

150

151

152

153

154

155

156

157

158

159

160

161

162

163

164

165

166

167

168

169

170

171

172

173

174

175

176

177

178

179

180

181

182

183

184

185

186

187

188

189

190

191

192

193

194

195

196

197

198

199

200

201

202

203

204

205

206

207

208

209

210

211

212

213

214

215

216

217

218

219

220

221

222

223

224

225

226

227

228

229

230

231

232

233

234

235

236

237

238

239

240

241

242

243

244

245

246

247

248

249

250

251

252

253

254

255

256

257

258

In one embodiment, the invention relates to any of the compoundsdepicted in Table 1 above and the pharmaceutically acceptable saltsthereof.

In another embodiment the invention relates to the group of compoundsdepicted in Table 1 consisting of compound number 1, 2, 3, 4, 5, 7, 8,9, 12, 15, 16, 18, 21, 27, 28, 30, 31, 35, 36, 39, 41, 42, 44, 45, 46,47, 48, 57, 59, 62, 68, 77, 78, 79, 80, 82, 83, 84, 85, 86, 88, 92, 93,and 94 and the pharmaceutically acceptable salts thereof.

In another embodiment the invention relates to the group of compoundsdepicted in Table 1 consisting of compound number 95, 97, 100, 101, 102,103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116,117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130,131, 132, 136, 137, 139, 140, 141, 142, 145, 146, 152, 153, 154, 155,157, 158, 159, 161, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172,173, 174, 175, 176, 177, 178, 179, 180, 181, 184, 185, 186, 187, 188,189, 191, 193, 194, 195, 196, 197, 198, 199, 201, 202, 203, 204, 205,206, 207, 208, 210, 211, 212, 213, 214, 215, 216, 220, 222, 223, 224,225, 227, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240,241, 242, 243, 244, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255,256, 257 and the pharmaceutically acceptable salts thereof.

Unless specifically indicated, throughout the specification and theappended claims, a given chemical formula or name shall encompasstautomers and all stereo, optical and geometrical isomers (e.g.enantiomers, diastereomers, E/Z isomers, etc.) and racemates thereof aswell as mixtures in different proportions of the separate enantiomers,mixtures of diastereomers, or mixtures of any of the foregoing formswhere such isomers and enantiomers exist, as well as salts, includingpharmaceutically acceptable salts thereof and solvates thereof such asfor instance hydrates including solvates of the free compounds orsolvates of a salt of the compound.

Some of the compounds of formula (I) can exist in more than onetautomeric form. The invention includes methods for using all suchtautomers.

The invention includes pharmaceutically acceptable derivatives ofcompounds of formula (I). A “pharmaceutically acceptable derivative”refers to any pharmaceutically acceptable salt or ester, or any othercompound which, upon administration to a patient, is capable ofproviding (directly or indirectly) a compound useful for the invention,or a pharmacologically active metabolite or pharmacologically activeresidue thereof. A pharmacologically active metabolite shall beunderstood to mean any compound of the invention capable of beingmetabolized enzymatically or chemically. This includes, for example,hydroxylated or oxidized derivative compounds of the formula (I).

As used herein, “pharmaceutically acceptable salts” refer to derivativesof the disclosed compounds wherein the parent compound is modified bymaking acid or base salts thereof. Examples of pharmaceuticallyacceptable salts include, but are not limited to, mineral or organicacid salts of basic residues such as amines; alkali or organic salts ofacidic residues such as carboxylic acids; and the like. For example,such salts include acetates, ascorbates, benzenesulfonates, benzoates,besylates, bicarbonates, bitartrates, bromides/hydrobromides, edetates,camsylates, carbonates, chlorides/hydrochlorides, citrates, edisylates,ethane disulfonates, estolates esylates, fumarates, gluceptates,gluconates, glutamates, glycolates, glycollylarsnilates,hexylresorcinates, hydrabamines, hydroxymaleates, hydroxynaphthoates,iodides, isothionates, lactates, lactobionates, malates, maleates,mandelates, methanesulfonates, methylbromides, methylnitrates,methylsulfates, mucates, napsylates, nitrates, oxalates, pamoates,pantothenates, phenylacetates, phosphates/diphosphates,polygalacturonates, propionates, salicylates, stearates, subacetates,succinates, sulfamides, sulfates, tannates, tartrates, teoclates,toluenesulfonates, triethiodides, ammonium, benzathines,chloroprocaines, cholines, diethanolamines, ethylenediamines, megluminesand procaines. Further pharmaceutically acceptable salts can be formedwith cations from metals like aluminium, calcium, lithium, magnesium,potassium, sodium, zinc and the like. (also see Pharmaceutical salts,Birge, S. M. et al., J. Pharm. Sci., (1977), 66, 1-19).

The pharmaceutically acceptable salts of the present invention can besynthesized from the parent compound which contains a basic or acidicmoiety by conventional chemical methods. Generally, such salts can beprepared by reacting the free acid or base forms of these compounds witha sufficient amount of the appropriate base or acid in water or in anorganic diluent like ether, ethyl acetate, ethanol, isopropanol, oracetonitrile, or a mixture thereof.

Salts of other acids than those mentioned above which for example areuseful for purifying or isolating the compounds of the present invention(e.g. trifluoro acetate salts) also comprise a part of the invention.

In addition, within the scope of the invention is use of prodrugs ofcompounds of the formula (I). Prodrugs include those compounds that,upon simple chemical transformation, are modified to produce compoundsof the invention. Simple chemical transformations include hydrolysis,oxidation and reduction. Specifically, when a prodrug is administered toa patient, the prodrug may be transformed into a compound disclosedhereinabove, thereby imparting the desired pharmacological effect.

The compounds of the invention are only those which are contemplated tobe ‘chemically stable’ as will be appreciated by those skilled in theart. For example, a compound which would have a ‘dangling valency’, or a‘carbanion’ are not compounds contemplated by the inventive methodsdisclosed herein.

For all compounds disclosed herein above in this application, in theevent the nomenclature is in conflict with the structure, it shall beunderstood that the compound is defined by the structure.

All terms as used herein in this specification, unless otherwise stated,shall be understood in their ordinary meaning as known in the art. Forexample, “C₁₋₄alkyl” is a saturated aliphatic hydrocarbon monovalentradical containing 1-4 carbons such as methyl, ethyl, n-propyl,1-methylethyl (isopropyl), n-butyl or t-butyl; “C₁₋₄ alkoxy” is a C₁₋₄alkyl with a terminal oxygen, such as methoxy, ethoxy, propoxy, butoxy.All alkyl, alkenyl and alkynyl groups shall be understood as beingbranched or unbranched, cyclized or uncyclized where structurallypossible and unless otherwise specified. Other more specific definitionsare as follows:

The term “C_(1-n)-alkyl”, wherein n is an integer from 2 to n, eitheralone or in combination with another radical denotes an acyclic,saturated, branched or linear hydrocarbon radical with 1 to n C atoms.For example the term C₁₋₅-alkyl embraces the radicals H₃C—, H₃C—CH₂—,H₃C—CH₂—CH₂—, H₃C—CH(CH₃)—, H₃C—CH₂—CH₂—CH₂—, H₃C—CH₂—CH(CH₃)—,H₃C—CH(CH₃)—CH₂—, H₃C—C(CH₃)₂—, H₃C—CH₂—CH₂—CH₂—CH₂—,H₃C—CH₂—CH₂—CH(CH₃)—, H₃C—CH₂—CH(CH₃)—CH₂—, H₃C—CH(CH₃)—CH₂—CH₂—,H₃C—CH₂—C(CH₃)₂—, H₃C—C(CH₃)₂—CH₂—, H₃C—CH(CH₃)—CH(CH₃)— andH₃C—CH₂—CH(CH₂CH₃)—.

The term “C_(1-n)-alkylene” wherein n is an integer 1 to n, either aloneor in combination with another radical, denotes an acyclic, straight orbranched chain divalent alkyl radical containing from 1 to n carbonatoms. For example the term C₁₋₄-alkylene includes —(CH₂)—, —(CH₂—CH₂)—,—(CH(CH₃))—, —(CH₂—CH₂—CH₂)—, —(C(CH₃)₂)—, —(CH(CH₂CH₃))—,—(CH(CH₃)—CH₂)—, —(CH₂—CH(CH₃))—, —(CH₂—CH₂—CH₂—CH₂)—,—(CH₂—CH₂—CH(CH₃))—, —(CH(CH₃)—CH₂—CH₂)—, —(CH₂—CH(CH₃)—CH₂)—,—(CH₂—C(CH₃)₂)—, —(C(CH₃)₂—CH₂)—, —(CH(CH₃)—CH(CH₃))—,—(CH₂—CH(CH₂CH₃))—, —(CH(CH₂CH₃)—CH₂)—, —(CH(CH₂CH₂CH₃))—,—(CHCH(CH₃)₂)— and —C(CH₃)(CH₂CH₃)—.

The term “C_(3-n)-cycloalkyl”, wherein n is an integer 4 to n, eitheralone or in combination with another radical denotes a cyclic,saturated, unbranched hydrocarbon radical with 3 to n C atoms. Forexample the term C₃₋₇-cycloalkyl includes cyclopropyl, cyclobutyl,cyclopentyl, cyclohexyl and cycloheptyl.

The term “heteroatom” as used herein shall be understood to mean atomsother than carbon such as O, N, S and P.

In all alkyl groups or carbon chains one or more carbon atoms can beoptionally replaced by heteroatoms: O, S or N, it shall be understoodthat if N is not substituted then it is NH, it shall also be understoodthat the heteroatoms may replace either terminal carbon atoms orinternal carbon atoms within a branched or unbranched carbon chain. Suchgroups can be substituted as herein above described by groups such asoxo to result in definitions such as but not limited to: alkoxycarbonyl,acyl, amido and thioxo.

The term “aryl” as used herein, either alone or in combination withanother radical, denotes a carbocyclic aromatic monocyclic groupcontaining 6 carbon atoms which may be further fused to a second 5- or6-membered carbocyclic group which may be aromatic, saturated orunsaturated. Aryl includes, but is not limited to, phenyl, indanyl,indenyl, naphthyl, anthracenyl, phenanthrenyl, tetrahydronaphthyl anddihydronaphthyl.

The term “heteroaryl” means an aromatic 5 to 6-membered monocyclicheteroaryl or an aromatic 7 to 11-membered heteroaryl bicyclic ringwhere at least one of the rings is aromatic, wherein the heteroaryl ringcontains 1-4 heteroatoms such as N, O and S, Non-limiting examples of 5to 6-membered monocyclic heteroaryl rings include furanyl, oxazolyl,isoxazolyl, oxadiazolyl, thiazolyl, pyrazolyl, pyrrolyl, imidazolyl,tetrazolyl, triazolyl, thienyl, thiadiazolyl, pyridinyl, pyrimidinyl,pyridazinyl, pyrazinyl, triazinyl, and purinyl. Non-limiting examples of7 to 11-membered heteroaryl bicyclic heteroaryl rings includebenzimidazolyl, quinolinyl, dihydro-2H-quinolinyl, isoquinolinyl,quinazolinyl, indazolyl, thieno[2,3-d]pyrimidinyl, indolyl, isoindolyl,benzofuranyl, benzopyranyl, benzodioxolyl, benzoxazolyl andbenzothiazolyl.

The term “heterocyclyl” means a stable nonaromatic 4-8 memberedmonocyclic heterocyclic radical or a stable non-aromatic 6 to11-membered fused bicyclic, bridged bicyclic or spirocyclic heterocyclicradical. The 5 to 11-membered heterocycle consists of carbon atoms andone or more, preferably from one to four heteroatoms chosen fromnitrogen, oxygen and sulfur. The heterocycle may be either saturated orpartially unsaturated. Non-limiting examples of nonaromatic 4-8 memberedmonocyclic heterocyclic radicals include tetrahydrofuranyl, azetidinyl,pyrrolidinyl, pyranyl, tetrahydropyranyl, dioxanyl, thiomorpholinyl,1,1-dioxo-1λ⁶-thiomorpholinyl, morpholinyl, piperidinyl, piperazinyl,and azepinyl. Non-limiting examples of nonaromatic 6 to 11-memberedfused bicyclic radicals include octahydroindolyl, octahydrobenzofuranyl,and octahydrobenzothiophenyl. Non-limiting examples of nonaromatic 6 to11-membered bridged bicyclic radicals include2-azabicyclo[2.2.1]heptanyl, 3-azabicyclo[3.1.0]hexanyl, and3-azabicyclo[3.2.1]octanyl. Non-limiting examples of nonaromatic 6 to11-membered spirocyclic heterocyclic radicals include7-aza-spiro[3,3]heptanyl, 7-spiro[3,4]octanyl, and7-aza-spiro[3,4]octanyl. The term “heterocyclyl” or is intended toinclude all the possible isomeric forms.

The term “halogen” as used in the present specification shall beunderstood to mean bromine, chlorine, fluorine or iodine. Thedefinitions “halogenated”, “partially or fully halogenated”; partiallyor fully fluorinated; “substituted by one or more halogen atoms”,includes for example, mono, di or tri halo derivatives on one or morecarbon atoms. For alkyl, a non-limiting example would be —CH₂CHF₂, —CF₃etc.

Each alkyl, cycloalkyl, heterocycle, aryl or heteroaryl, or the analogsthereof, described herein shall be understood to be optionally partiallyor fully halogenated.

As used herein, “nitrogen” or N and “sulfur” or S includes any oxidizedform of nitrogen and sulfur and the quaternized form of any basicnitrogen. For example, for an —S—C₁₋₆ alkyl radical, unless otherwisespecified, this shall be understood to include —S(O)—C₁₋₆ alkyl and—S(O)₂—C₁₋₆ alkyl, likewise, —S—R_(a) may be represented asphenyl-S(O)_(m)— when R_(a) is phenyl and where m is 0, 1 or 2.

General Synthetic Methods

The compounds of the invention may be prepared by the general methodsand examples presented below and methods known to those of ordinaryskill in the art. Optimum reaction conditions and reaction times mayvary depending on the particular reactants used. Unless otherwisespecified, solvents, temperatures, pressures, and other reactionconditions may be readily selected by one of ordinary skill in the art.Specific procedures are provided in the Synthetic Examples section.Intermediates used in the syntheses below are either commerciallyavailable or easily prepared by methods known to those skilled in theart. Reaction progress may be monitored by conventional methods such asthin layer chromatography (TLC) or high pressure liquidchromatography-mass spec (HPLC-MS). Intermediates and products may bepurified by methods known in the art, including column chromatography,HPLC, preparative TLC or recrystallization.

The methods described below and in the Synthetic Examples section may beused to prepare the compounds of formula I.

Compounds of formula I may be prepared as described in Scheme 1

As illustrated above, diester II (R=Me or Et) and hydrazine III arerefluxed in a suitable solvent such as ethanol with a suitable base suchas potassium carbonate (K₂CO₃) yielding hydroxy pyrazole IV. Compound IVis alkylated, for example by using trimethylsilyldiazomethane in somecases or R¹I and a suitable base such as cesium carbonate (Cs₂CO₃).Alternatively, Mitsunobu conditions are employed with ethanol to yieldthe desired alkoxy pyrazole chloropyridine V (R′=Et). Chloropyridine, V,is coupled with boron species, VI, in the presence of a palladiumcatalyst such as tetrakis(triphenyl) phosphine (0) and a suitable basesuch as Na₂CO₃ in aqueous 1,2-DME (1,2-dimethoxyethane) under microwaveirradiation at 120° C. to provide VII. Alkylation of the phenolintermediate, VII with alkyl bromide VIII, where X═Cl, I or Br using abase such as cesium carbonate (Cs₂CO₃) in a solvent such as acetone atabout 50° C. Subsequent deprotection of the t-Boc group with a suitableacid such as trifluoroacetic acid (TFA) provides compound IX. Reductiveamination of amine, IX, with the desired ketone or aldehyde using anappropriate hydride source such as NaBH₃CN in a solvent such as MeOHcontaining an organic acid such as AcOH at about 50° C., followed by insitu hydrolysis with a base such as aqueous LiOH affords the desiredcompound of formula I. Alternatively, alkylations of amine, IX withalkyl halides in the presence of a suitable base such as cesiumcarbonate (Cs₂CO₃) or N,N-diisopropylethylamine (DIPEA) in a solventsuch as MeCN (acetonitrile) followed by hydrolysis of the ester providesthe desired compound of formula I.

UPLC/MS Methods

Retention times (RT) reported for compounds in the Synthetic Examplessection are obtained by UPLC/MS using one of the following methods:

For each of the methods, the following are identical:

UPLC/MS system components—Acquity UPLC with PDA, SQ and ELS detectors.

PDA conditions—Detection: 210 to 400 nm. Sampling rate: 20 pts/sec.Filter response: fast.

ELSD conditions—Gain: 1000. Sampling rate: 20 pts/sec. Drift tube temp:55° C. Nebulizer mode: cooling. Gas pressure: 41 psi.

MS conditions—Instrument: Acquity SQD with ESCi source. Ionization mode:ESI+/−.

Capillary voltage: 3.5 kV. Cone voltage: 5 V. Extractor: 1.3 V. Sourcetemp: 150° C.

Desolvation temp: 350° C. Desolvation gas: 800 L/hr. Cone gas: 50 L/hr.

Conditions specific to each method are as follows

Method A1

Column—Waters BEH C18, 2.1×50 mm, 1.7 um particle diameter.

Description and Gradient: Medium polar fast gradient method. ESI+/− ionmode 80-1000 Da.

Gradient: 90% A to 100% B in 1.19 minutes hold at 100% B to 1.70minutes. Flow rate 0.8 mL/min. A=(95% Water 5% Acetonitrile 0.05% FormicAcid) B=(Acetonitrile 0.05% Formic Acid).

Sample Injection Volume: 1 uL

Method A2

Column—Waters BEH C18, 2.1×50 mm, 1.7 um particle diameter.

Description and Gradient: Medium polar long gradient method. ESI+/− ionmode 80-1000 Da.

Gradient: 90% A to 100% B in 4.45 minutes hold at 100% B to 4.58minutes. Flow rate 0.8 mL/min. A=(95% Water 5% Acetonitrile 0.05% FormicAcid) B=(Acetonitrile 0.05% Formic Acid).

Sample Injection Volume: 2 uL

Method B1

Column—CSH 2.1×50 mm C18, 1.7 um particle diameter.

Description and Gradient: Medium polar fast gradient method. ESI+/− ionmode 80-1000 Da.

Gradient: 90% A to 100% B in 1.19 minutes hold at 100% B to 1.70minutes. Flow rate 0.8 mL/min. A=(95% Water 5% Acetonitrile 0.05% FormicAcid) B=(Acetonitrile 0.05% Formic Acid).

Sample Injection Volume: 1 uL

Method B2

Column—CSH 2.1×50 mm C18, 1.7 um particle diameter.

Description and Gradient: Medium polar long gradient method. ESI+/− ionmode 80-1000 Da.

Gradient: 90% A to 100% B in 4.45 minutes hold at 100% B to 4.58minutes. Flow rate 0.8 mL/min. A=(95% Water 5% Acetonitrile 0.05% FormicAcid) B=(Acetonitrile 0.05% Formic Acid).

Sample Injection Volume: 2 uL

Method A1 is used for all of the compounds except for compounds notedfor which Method A2, Method B1, or Method B2 is used.

SYNTHETIC EXAMPLES

Final compounds are designated by compound numbers corresponding to thecompound numbers in Table 1. Intermediates are given hyphenated numberscorresponding to the figures and numbers shown in the scheme for eachexample.

Example 1 Preparation of intermediate1-[6-(2-hydroxy-3-methyl-phenyl)-pyridin-2-yl]-5-isopropoxy-1H-pyrazole-4-carboxylicacid ethyl ester (1-6)

To a round bottom flask containing EtOH (200 mL), K₂CO₃ (20.05 g, 55.720mmol), and 1-1 (10.00 g, 69.65 mmol) is added 1-2 (13.95 mL, 69.65mmol). The resulting mixture is refluxed for 3 h. The reaction is cooledand the solid is collected by filtration. This solid is removed from thefritted funnel and is placed into a beaker to which is added 250 mL of1.0 N HCl (excessive bubbling). The solution is confirmed to be acidic(pH 2) and then dichloromethane (500 mL) is added. The mixture isstirred until all solid is dissolved. The organic layer is collected,dried over MgSO₄, and concentrated to afford 1-3 (17.18 g) as anoff-white solid.

A reaction mixture of 1-3 (0.50 g, 1.87 mmol), 2-iodopropane (372.92 μL,3.74 mmol), Cs₂CO₃ (0.91 g, 2.80 mmol) in DMA (9.0 mL) is heated at 150°C. in a microwave reactor for 10 min. The mixture is added to water andis extracted with EtOAc (2×). The organic layers are washed with water,brine, dried over MgSO₄, and concentrated. The crude is purified bysilica gel chromatography using a gradient of 12-100% EtOAc in heptaneto yield the desired product 1-4 (0.41 g).

To a microwave vial is added 1-4 (1.00 g, 3.29 mmol), 1-5 (0.69 g, 4.52mmol), Pd(PPh₃)₄ (0.37 g, 0.32 mmol), DME (15.0 mL), and 2.0 M Na₂CO₃(4.36 mL, 8.72 mmol). The reaction mixture is heated in microwavereactor at 120° C. for 20 min. The reaction is extracted withdichloromethane (2×), washed with water, brine, dried over Na₂SO₄, andconcentrated. The resulting material is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptane to yield thedesired product 1-6 (0.41 g).

Example 2 Preparation of intermediate1-[6-(2-hydroxy-3-methyl-phenyl)-pyridin-2-yl]-5-methoxy-1H-pyrazole-4-carboxylic acid ethyl ester (2-8)

Intermediate 1-3 (7.00 g, 26.15 mmol) is dissolved in 1:1 mixtureEtOAc/MeOH (50.0 mL). 2.0 M TMSCHN₂ in hexanes (42.70 mL, 85.40 mmol) isthen added slowly via a syringe. The reaction is stirred for 3 h and isquenched by the addition of acetic acid (4.0 mL). The mixture is stirredfor 10 min and then concentrated. The resulting residue is purified bysilica gel chromatography using a gradient of 12-100% EtOAc in heptaneto yield the desired product 2-7 (4.460 g) as an off-white solid.

To a microwave vial is added 2-7 (1.50 g, 5.33 mmol), 1-5 (0.890 g, 5.86mmol), Pd(PPh₃)₄ (0.62 g, 0.532 mmol), DME (12.0 mL), and 2.0 M Na₂CO₃(6.922 mL, 13.85 mmol). The reaction mixture is heated in a microwavereactor at 120° C. for 20 min. The reaction is extracted withdichloromethane (2×), washed with water, brine, dried over MgSO₄, andconcentrated. The resulting material is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptane to yield thedesired product 2-8 (1.17 g).

The following intermediates are synthesized in a similar fashion fromthe appropriate reagents:

Example 3 Preparation of intermediate5-ethoxy-1-[6-(2-hydroxy-3-methyl-phenyl)-pyridin-2-yl]-1H-pyrazole-4-carboxylicacid ethyl ester (3-15)

1-(6-Chloro-pyridin-2-yl)-5-hydroxy-1H-pyrazole-4-carboxylic acid ethylester, 1-3, (3.50 g, 13.08 mmol) is dissolved in THF (90.0 mL).Triphenylphosphine (3.77 g, 14.383 mmol) and ethanol (1.14 mL, 19.614mmol) are added and the reaction is cooled to 0° C. The resultingsuspension is slowly dissolved at 0° C. as diisopropyl azodicarboxylate(3.09 mL, 15.691 mmol) is added dropwise over 10 min. The reactionmixture is allowed to warm to ambient temperature and is stirred for 16h. The reaction is concentrated in vacuo and the residue is dissolved ina minimal amount of dichloromethane and subjected to silica gelchromatography using a gradient of 3-50% EtOAc in heptane to yield thedesired product 3-14 (3.33 g).

To a microwave vial is added 3-14 (250.0 mg, 0.85 mmol), 1-5 (134.9 mg,0.89 mmol), Pd(PPh₃)₄ (60.05 mg, 0.05 mmol), DME (5.0 mL), and 2.0 MNa₂CO₃ (1.06 mL, 2.11 mmol). The reaction mixture is heated in amicrowave reactor at 120° C. for 20 min. The reaction is extracted withdichloromethane (2×), washed with water, brine, dried over MgSO₄, andconcentrated. The resulting material is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptane to yield thedesired product, 3-15 (227.0 mg).

The following intermediate is synthesized in a similar fashion from theappropriate reagents:

Example 4 Preparation of intermediate6-bromomethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butylester (4-19)

Compound 4-17 (12.50 g, 45.08 mmol) is dissolved in dry THF (125.0 mL)under nitrogen at 25° C. Borane THF complex (99.17 mL, 99.17 mmol) isadded via syringe and the mixture is stirred at 25° C. for 16 h. Water(10.0 mL) is slowly added and then 2.0 M Na₂CO₃ (15.0 mL). This mixtureis stirred for 15 min and then is diluted with EtOAc and the organiclayers are collected. The organics are rinsed with 1.0 M HCl, dried overMgSO₄, and concentrated in vacuo to afford an oil. The oil is purifiedby silica gel chromatography using a gradient of 10-80% EtOAc in heptaneto yield the desired product, 4-18 (11.78 g), as a white solid.

To a solution of alcohol, 4-18, (9.50 g, 36.08 mmol) andN,N-diisopropylethylamine (9.43 mL, 54.11 mmol) in dichloromethane(200.0 mL) is added triphenylphosphine dibromide (23.79 g, 54.11 mmol)at 0° C. The reaction is stirred for 1 h and concentrated in vacuo. Theresulting residue is purified by silica gel chromatography using agradient of 7-60% EtOAc in heptanes to yield the desired product, 4-19(8.74 g), as a white solid.

The following intermediates are synthesized in similar fashion from theappropriate reagents:

Example 5 Preparation of intermediate6-bromomethyl-5-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester (5-34)

A solution of acid 5-23 (350.0 g, 2.10 mol) in THF (1.4 L) is added to aslurry of LAH (95.9 g, 1.40 mol) in THF (2.5 L) at 0° C. The mixture isstirred at room temperature for 0.5 h, then heated to reflux for 1 h.The mixture is then cooled to 0° C., and slowly quenched by the additionof saturated aqueous ammonium chloride solution. A large excess of solidNa₂SO₄ and EtOAc are added, then the solids are collected by filtration.The filtrate is concentrated in vacuo to afford crude 5-24 (350.0 g)which is used directly in the next step.

To a solution of compound 5-24 (294.0 g, 1.90 mol) in dichloromethane(2.2 L) at −10° C. is added thionyl chloride (SOCl₂) (460.0 g, 3.90mol). Then the reaction mixture is heated to reflux for 1 h, followed byconcentration in vacuo to provide crude 5-25 (298.0 g) which is useddirectly in the next step.

A mixture of compound 5-25 (298.0 g, 1.8 mol) and NaCN (154.5 g, 2.1mol) in DMF (1.2 L) is stirred at room temperature for 12 h, thenextracted with EtOAc and H₂O. The organic layer is dried over Na₂SO₄,filtered, and concentrated in vacuo. The residue is purified by silicagel chromatography (petroleum ether:EtOAc=50:1) to deliver intermediate5-26 (230.0 g).

A mixture of compound 5-26 (180.0 g, 1.10 mol), Raney Ni (40.0 g) andaqueous ammonia (250.0 mL) in MeOH (1.0 L) is stirred under H₂ (50 psi)at room temperature for 5 h. The mixture is then filtered andconcentrated to give compound 5-27 (165.0 g) that is used directly inthe next step.

A solution of compound 5-27 (165.0 g, 1.0 mol) and aqueous formaldehyde(HCHO) (37 wt %, 30 g, 1.0 mol) in formic acid (HCO₂H) (1.5 L) isstirred at 50° C. overnight, then the solvent is removed in vacuo toafford compound 5-28 (150.0 g) which is used directly in the next step.

Compound 5-28 (150.0 g, 847 mmol) is suspended in aqueous HBr (48%, 1.0L), then heated to 100° C. overnight. Removal of the solvent in vacuoprovides compound 5-29 (195.0 g) which is used directly in the nextstep.

To a solution of compound 5-29 (195.0 g, 799 mmol) in THF (1.0 L) andH₂O (1.0 L) is added Et₃N (242.0 g, 2.4 mol) and Boc₂O (174.0 g, 799mmol). The resulting mixture is stirred at room temperature overnight,then extracted with EtOAc. The combined organic phases are washed withbrine, dried over Na₂SO₄, filtered and concentrated in vacuo. The crudeproduct is purified by silica gel chromatography (using 10:1 petroleumether:EtOAc) to provide compound 5-30 (100.0 g).

To a solution of compound 5-30 (100.0 g, 380 mmol) and Et₃N (76.8 g, 760mmol) in dichloromethane (1.5 L) cooled to 0° C. is added triflicanhydride (Tf₂O) (107.0 g, 380 mmol) via addition funnel. Upon completeaddition of Tf₂O, the solution is warmed to room temperature for 5 h.The reaction mixture is then treated with H₂O and dichloromethane, andthe organic phase is separated, washed with brine, dried over Na₂SO₄,filtered, and concentrated in vacuo. The residue is purified by silicagel chromatography (using 20:1 petroleum ether:EtOAc) to providecompound 5-31 (105.0 g).

Compound 5-31 (50.0 g, 127 mmol) is combined with palladium (II) acetate(Pd(OAc)₂) (5.0 g), dppp (5.0 g) and Et₃N (25.7 g, 254 mmol) in EtOH(1.0 L), then stirred at 80° C. overnight under CO at a pressure of 4MPa. The mixture is cooled to room temperature, then the solids areremoved by filtration. The filtrate is concentrated in vacuo, and theremaining residue is purified by silica gel chromatography (using 20:1petroleum ether:EtOAc) to provide compound 5-32 (25.0 g).

To a solution of LAH (12.5 g, 330 mmol) in THF (400 mL) cooled to −30°C. is added dropwise a solution of compound 5-32 (35.0 g, 110 mmol) inTHF (400 mL) over 30 min. After addition, the reaction mixture isstirred at 0° C. for 30 min, then treated with H₂O and dichloromethane.The organic phase is separated, washed with brine, dried over Na₂SO₄,filtered, and concentrated in vacuo. The crude product is purified bysilica gel chromatographyl (using 10:1 petroleum ether:EtOAc) to providethe desired intermediate 5-33 (21.1 g).

To a solution of alcohol, 5-33, (6.00 g, 21.63 mmol) andN,N-diisopropylethylamine (5.65 mL, 32.45 mmol) in dichloromethane(200.0 mL) is added triphenylphosphine dibromide (14.27 g, 32.45 mmol)at 0° C. The reaction is stirred for 1 h and concentrated in vacuo. Theresulting residue is purified by silica gel chromatography using agradient of 7-60% EtOAc in heptanes to yield the desired product, 5-34(6.60 g), as a white solid.

Example 6 Preparation of intermediate6-Bromomethyl-5-chloro-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester (6-39)

To a solution of N,N,N′-trimethyl-ethane-1,2-diamine (45.0 g, 442.0mmol) in THF (500 mL) is added a solution of n-BuLi (177.0 mL, 442 mmol)at −40° C. under N₂. The mixture is stirred at −40° C. for 30 min. Afterthe mixture is cooled to −70° C., compound 6-35 (50.0 g, 368 mmol) inTHF (250 mL) is added to the reaction mixture. The mixture is allowed towarm to 0° C. and stirred for 30 min. Then the reaction mixture iscooled to −78° C. and n-BuLi (177.0 mL, 442 mmol) is added. The mixtureis allowed to warm to 10° C. and is cooled to −30° C. before it is addedto a solution of C₂Cl₆ (287.0 g, 1.1 mol) in THF (600 mL). The mixtureis stirred 2 h at room temperature. The reaction mixture is poured into1000 mL of 10% HCl solution and extracted with EtOAc. The organic layersare washed with brine, dried over Na₂SO₄, concentrated, and purified bysilica gel chromatography to give compound 6-36 (36.7 g).

To a solution of compound 6-36 (105.0 g, 615 mmol) in HOAc (700 mL) isadded NH₄OAc (47.4 g, 615 mmol) at room temperature under N₂. To thisreaction mixture is added MeNO₂ (188.0 g, 3.08 mol) and the mixture iswarmed to 40° C. for 12 h and then is stirred at 85° C. for 6 h. TLCshowed the reaction is completed. The mixture is quenched with H2O andis extracted with dichloromethane. The organic layers are washed withbrine, dried over Na2SO4, concentrated, and purified by silica gelchromatography to give compound 6-37 (97.5 g).

To a solution of compound 6-37 (48.0 g, 225 mmol) in THF (900 mL) isadded LAH (34.1 g, 899 mol) at −20° C. The mixture is stirred at roomtemperature for 5 h and 50° C. for 30 min. The mixture is quenched withH₂O and is extracted with dichloromethane. The organic layers are washedwith brine, dried over Na₂SO₄, and concentrated to give compound 6-38(28.0 g) which is used directly in the next step.

The following compound is prepared from intermediate 6-38 according tothe procedure described in Example 5:

Example 7 Preparation of5-isopropoxy-1-(6-{3-methyl-2-[2-(tetrahydro-pyran-4-yl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (1)

Intermediate 1-6 (373.0 mg, 0.88 mmol), bromide 4-19 (287.1 mg, 0.88mmol) and Cs₂CO₃ (573.5 mg, 1.76 mmol) are combined in acetone (11.0 mL)and heated to 50° C. for 5 h. The reaction mixture is extracted withEtOAc, washed with brine, dried over MgSO₄, and concentrated. Theresulting material is purified by silica gel chromatography (using agradient of 5-100% EtOAc/heptane) to provide the desired intermediate,7-40 (502.0 mg).

The carbamate, 7-40, (496.0 mg, 0.79 mmol) is dissolved indichloromethane (4.0 mL) and treated with TFA (1.0 mL) at roomtemperature. After 1 h the mixture is neutralized with saturated NaHCO₃solution and the layers are separated with a hydrophobic frit. Theorganic filtrate is concentrated to afford 7-41 (375.0 mg).

Amine 7-41 (98.0 mg, 0.19 mmol) is combined with 4 Å molecular sieves(30 mg), tetrahydropyran 4-one (28 μL, 0.28 mmol), AcOH (20 μL), andNa(CN)BH₃ (24 mg, 0.38 mmol) in MeOH (4 mL). The mixture is stirred atroom temperature for 30 min, and then heated to 50° C. for 12 h. Themixture is diluted with THF (1.0 mL) and water (1 mL). To this is addedLiOH (42.8 mg, 1.86 mmol) and the reaction is heated to 50° C. for 2 h.It is then concentrated under N₂, triturated with 1:1 MeOH/DMSO,filtered through a 0.45 micron syringe filter, and the filtrate ispurified by gradient elution (10-100% MeCN/water+0.1% HCO₂H) on a GilsonRP-HPLC. Concentrated in vacuo to afford title compound 1 (64.0 mg). MS,electrospray, m/z=583.3 [M+H], RT 0.71 min.

Example 7A Procedure is equivalent to Example 7, however duringreductive amination step Na(OAc)₃BH in dichloromethane is substitutedfor NaCNBH₃/AcOH/MeOH.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using the appropriate startingmaterials and purification conditions

Compound 2: MS, electrospray, m/z=617.3 [M+H], RT 0.79 min;

Compound 37: MS, electrospray, m/z=541.3 [M+H], RT 0.75 min;

Compound 38: MS, electrospray, m/z=571.4 [M+H], RT 0.76 min;

Compound 39: MS, electrospray, m/z=555.3 [M+H], RT 0.73 min;

Compound 40: MS, electrospray, m/z=583.3 [M+H], RT 0.73 min;

Compound 41: MS, electrospray, m/z=569.3 [M+H], RT 0.73 min;

Compound 42: MS, electrospray, m/z=583.3 [M+H], RT 0.75 min;

Compound 109: MS, electrospray, m/z=569.4 [M+H], RT 0.77 min;

Resolution: ChiralPak AD-H Prep 40% i-Propanol(1% iPrNH₂):CO₂ @ 80ml/min., 100 bar, 25° C.

Compound 111: MS, electrospray, m/z=569.4 [M+H], RT 0.77 min;

Resolution: ChiralPak AD-H Prep 40% i-Propanol(1% iPrNH₂):CO₂ @ 80ml/min., 100 bar, 25° C.

Compound 113: MS, electrospray, m/z=583.3 [M+H], RT 0.75 min;

Resolution: Lux Cellulose 2 Prep 60% MeOH (1% iPrNH₂): CO₂ @ 55 ml/min.,100 bar, 25° C.

Compound 115: MS, electrospray, m/z=583.3 [M+H], RT 0.75 min;

Resolution: Lux Cellulose 2 Prep 60% MeOH (1% iPrNH₂): CO₂ @ 55 ml/min.,100 bar, 25° C.

Compound 144: MS, electrospray, m/z=569.4 [M+H], RT 0.77 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 1-6, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 43: MS, electrospray, m/z=555.4 [M+H], RT 0.77 min;

Compound 44: MS, electrospray, m/z=585.4 [M+H], RT 0.80 min;

Compound 45: MS, electrospray, m/z=569.3 [M+H], RT 0.75 min;

Compound 46: MS, electrospray, m/z=597.4 [M+H], RT 0.76 min;

Compound 47: MS, electrospray, m/z=583.3 [M+H], RT 0.76 min;

Compound 48: MS, electrospray, m/z=597.4 [M+H], RT 0.77 min;

Compound 104: MS, electrospray, m/z=597.5 [M+H], RT 0.80 min;

Compound 116: MS, electrospray, m/z=597.4 [M+H], RT 0.77 min;

Resolution: Lux Cellulose 2 Prep 65% MeOH (1% iPrNH₂): CO₂ @ 60 ml/min.,125 bar, 25° C.

Compound 117: MS, electrospray, m/z=597.4 [M+H], RT 0.77 min;

Resolution: Lux Cellulose 2 Prep 65% MeOH (1% iPrNH₂): CO₂ @ 60 ml/min.,125 bar, 25° C.

Compound 122: MS, electrospray, m/z=581.5 [M+H], RT 0.72 min;

Resolution: RegisPack Prep 15% IPA (1% diethylamine): CO₂ @ 12 ml/min.,120 bar, 40° C.

Compound 123: MS, electrospray, m/z=581.5 [M+H], RT 0.72 min.

Resolution: RegisPack Prep 15% IPA (1% diethylamine): CO₂ @ 12 ml/min.,120 bar, 40° C.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 3: MS, electrospray, m/z=555.3 [M+H], RT 0.64 min;

Compound 5: MS, electrospray, m/z=587.2 [M−H], RT 0.78 min;

Compound 8: MS, electrospray, m/z=527.2 [M+H], RT 0.69 min;

Compound 12: MS, electrospray, m/z=555.3 [M+H], RT 0.68 min;

Compound 13: MS, electrospray, m/z=513.2 [M+H], RT 0.70 min;

Compound 14: MS, electrospray, m/z=541.3 [M+H], RT 0.77 min;

Compound 15: MS, electrospray, m/z=541.2 [M+H], RT 0.68 min;

Compound 23: MS, electrospray, m/z=543.3 [M+H], RT 0.70 min;

Compound 24: MS, electrospray, m/z=525.2 [M+H], RT 0.72 min;

Compound 25: MS, electrospray, m/z=539.3 [M+H], RT 0.75 min;

Compound 61: MS, electrospray, m/z=583.3 [M+H], RT 0.72 min;

Compound 62: MS, electrospray, m/z=583.4 [M+H], RT 0.72 min;

Compound 73: MS, electrospray, m/z=611.4 [M+H], RT 0.75 min;

Compound 75: MS, electrospray, m/z=593.4 [M−H], RT 0.72 min;

Compound 81: MS, electrospray, m/z=585.1 [M+H], Method A2, RT 1.42 min;

Compound 86: MS, electrospray, m/z=569.4 [M+H], RT 0.78 min;

Compound 87: MS, electrospray, m/z=581.4 [M+H], RT 0.80 min;

Compound 90: MS, electrospray, m/z=583.4 [M+H], RT 0.80 min;

Compound 91: MS, electrospray, m/z=583.4 [M+H], RT 0.83 min;

Compound 92: MS, electrospray, m/z=571.4 [M+H], RT 0.79 min;

Compound 102: MS, electrospray, m/z=609.4 [M+H], RT 0.83 min;

Compound 103: MS, electrospray, m/z=609.4 [M+H], RT 0.89 min;

Compound 188: MS, electrospray, m/z=555.3 [M+H], RT 0.58 min;

Compound 192: MS, electrospray, m/z=555.3 [M+H], RT 0.58 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 4-20, andother appropriate starting materials and purification conditions:

Compound 10: MS, electrospray, m/z=555.2 [M+H], RT 0.82 min;

Compound 89: MS, electrospray, m/z=583.4 [M+H], Method A2, RT 1.80 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 4-20, andother appropriate starting materials and purification conditions:

Compound 217: MS, electrospray, m/z=569.3 [M+H], 1.45 min (method B2);

Compound 218: MS, electrospray, m/z=583.3 [M+H], 1.52 min (method B2);

Compound 219: MS, electrospray, m/z=599.3 [M+H], 1.46 min (method B2);

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 4-21, andother appropriate starting materials and purification conditions:

Compound 59: MS, electrospray, m/z=541.3 [M+H], RT 0.66 min;

Compound 85: MS, electrospray, m/z=513.2 [M+H], RT 0.71 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 4-22, andother appropriate starting materials and purification conditions:

Compound 100: MS, electrospray, m/z=569.4 [M+H], RT 0.77 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 4-23, andother appropriate starting materials and purification conditions:

Compound 130: MS, electrospray, m/z=571.4 [M+H], RT 0.69 min (MethodB1);

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 16: MS, electrospray, m/z=541.2 [M+H], RT 0.70 min;

Compound 27: MS, electrospray, m/z=569.3 [M+H], RT 0.70 min;

Compound 28: MS, electrospray, m/z=569.3 [M+H], RT 0.70 min;

Compound 30: MS, electrospray, m/z=555.3 [M+H], RT 0.77 min;

Compound 31: MS, electrospray, m/z=555.3 [M+H], RT 0.70 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 105: MS, electrospray, m/z=555.4 [M+H], RT 0.72 min

Resolution: Chirapak AD-H, 20×250 mm; MeOH to 30 mg/mL, 35% EtOH (1%DEA) in heptane over 18 min, ambient temp. and collection at 290 nm;

Compound 106: MS, electrospray, m/z=555.4 [M+H], RT 0.72 min

Resolution: Chirapak AD-H, 20×250 mm; MeOH to 30 mg/mL, 35% EtOH (1%DEA) in heptane over 18 min, ambient temp. and collection at 290 nm;

Compound 127: MS, electrospray, m/z=569.4 [M+H], RT 0.76 min;

Compound 139: MS, electrospray, m/z=585.4 [M+H], RT 0.74 min

Resolution: Chiracel OD-H, 20×250 mm; 10% MeOH in CO₂ at 55.5 g/min over28 min, 140 Bar, 40° C. and collection at 254 nm;

Compound 140: MS, electrospray, m/z=569.4 [M+H], RT 0.74 min

Resolution: Chiracel OD-H, 20×250 mm; 10% MeOH in CO₂ at 58 g/min over30 min, 120 Bar, 40° C. and collection at 254 nm;

Compound 141: MS, electrospray, m/z=569.4 [M+H], RT 0.74 min

Resolution: Chiracel OD-H, 20×250 mm; 10% MeOH in CO₂ at 58 g/min over30 min, 120 Bar, 40° C. and collection at 254 nm;

Compound 142: MS, electrospray, m/z=585.4 [M+H], RT 0.74 min

Resolution: Chiracel OD-H, 20×250 mm; 10% MeOH in CO₂ at 55.5 g/min over28 min, 140 Bar, 40° C. and collection at 254 nm;

Compound 191: MS, electrospray, m/z=569.3 [M+H], RT 0.61 min;

Compound 198: MS, electrospray, m/z=583.3 [M+H], RT 0.66 min (methodB1);

Resolution: LUX Amylose-2, 21×250 mm 35% (1:1:1MeOH:EtOH:iPA)+Et₂NH:CO₂, 80 ml/min, 110 bar, 40° C.

Compound 199: MS, electrospray, m/z=583.3 [M+H], RT 0.66 min (methodB1).

Resolution: LUX Amylose-2, 21×250 mm 35% (1:1:1MeOH:EtOH:iPA)+Et₂NH:CO₂, 80 ml/min, 110 bar, 40° C.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-8, bromide, 6-39, andother appropriate starting materials and purification conditions:

Compound 17: MS, electrospray, m/z=561.2 [M+H], RT 0.77 min;

Compound 18: MS, electrospray, m/z=589.3 [M+H], RT 0.73 min;

Compound 19: MS, electrospray, m/z=589.3 [M+H], RT 0.73 min;

Compound 20: MS, electrospray, m/z=559.3 [M+H], RT 0.76 min;

Compound 21: MS, electrospray, m/z=575.3 [M+H], RT 0.83 min;

Compound 22: MS, electrospray, m/z=575.3 [M+H], RT 0.73 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-9, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 7: MS, electrospray, m/z=547.2 [M+H], RT 0.71 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-10, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 9: MS, electrospray, m/z=581.2 [M+H], RT 0.73 min;

Compound 83: MS, electrospray, m/z=609.4 [M+H], RT 0.79 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-10, bromide, 4-21, andother appropriate starting materials and purification conditions:

Compound 93: MS, electrospray, m/z=595.3 [M+H], RT 0.80 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-10, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 84: MS, electrospray, m/z=623.4 [M+H], RT 0.83 min;

Compound 88: MS, electrospray, m/z=595.3 [M+H], RT 0.80 min;

Compound 107: MS, electrospray, m/z=607.4 [M+H], RT 0.77 min;

Resolution: Chirapak AD-H, 30×250 mm; 50% Isopropanol: Hexane with 1%Isopropylamine @ 88 mL/min, 100 bar CO₂, ambient temp.

Compound 108: MS, electrospray, m/z=607.4 [M+H], RT 0.77 min.

Resolution: Chirapak AD-H, 30×250 mm; 50% Isopropanol: Hexane with 1%Isopropylamine @ 88 mL/min, 100 bar CO₂, ambient temp.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 2-11, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 52: MS, electrospray, m/z=547.3 [M−H], RT 0.70 min;

Compound 53: MS, electrospray, m/z=575.3 [M−H], RT 0.71 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-12, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 63: MS, electrospray, m/z=559.3 [M+H], RT 0.65 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-13, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 98: MS, electrospray, m/z=555.4 [M+H], RT 0.76 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 2-13, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 99: MS, electrospray, m/z=569.4 [M+H], RT 0.79 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-14, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 124: MS, electrospray, m/z=569.4 [M+H], RT 0.71 min

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 3-15, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 6: MS, electrospray, m/z=541.2 [M+H], RT 0.73 min;

Compound 32: MS, electrospray, m/z=527.3 [M+H], RT 0.73 min;

Compound 34: MS, electrospray, m/z=569.3 [M+H], RT 0.71 min;

Compound 35: MS, electrospray, m/z=555.3 [M+H], RT 0.71 min;

Compound 36: MS, electrospray, m/z=569.3 [M+H], RT 0.73 min;

Compound 110: MS, electrospray, m/z=555.4 [M+H], RT 0.75 min;

Resolution: ChiralPak AD-H Prep 30% EtOH:CO₂ @ 80 ml/min., 100 bar, 25°C.

Compound 112: MS, electrospray, m/z=555.4 [M+H], RT 0.75 min.

Resolution: ChiralPak AD-H Prep 30% EtOH:CO₂ @ 80 ml/min., 100 bar, 25°C.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 3-15, bromide, 4-22, andother appropriate starting materials and purification conditions:

Compound 245: MS, electrospray, m/z=583.1 [M+H], RT 0.62 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7, using phenol, 3-15, bromide, 4-23, andother appropriate starting materials and purification conditions:

Compound 131: MS, electrospray, m/z=585.4 [M+H], RT 1.21 min (MethodB1);

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 3-15, bromide, 4-24, andother appropriate starting materials and purification conditions:

Compound 205: MS, electrospray, m/z=583.3 [M+H], RT 0.67 min (MethodB1);

Compound 213: MS, electrospray, m/z=555.3 [M+H], RT 0.67 min (MethodB1);

The following compounds from Table 1 are prepared according to theprocedure described in Example 7, using phenol, 3-15, bromide, 5-34, andother appropriate starting materials and purification conditions:

Compound 114: MS, electrospray, m/z=583.5 [M+H], RT 0.62 min;

Compound 125: MS, electrospray, m/z=569.4 [M+H], RT 1.25 min (MethodB2);

Resolution: LUX 5 u Cellulose 2 Prep, 23% MeOH (1% Et2NH) in CO2 at 78ml/min over 21 minutes, 160 Bar, 40° C.

Compound 126: MS, electrospray, m/z=569.4 [M+H], RT 1.25 min (MethodB2);

Resolution: LUX 5 u Cellulose 2 Prep, 23% MeOH (1% Et2NH) in CO2 at 78ml/min over 21 minutes, 160 Bar, 40° C.

Compound 128: MS, electrospray, m/z=583.5 [M+H], RT 1.31 min (MethodB2);

Resolution: Chiralcel OD-H, 20×250 mm 5.8% MeOH (˜1% Et2NH) in CO2 at 85g/min, 160 Bar, 40 C.

Compound 129: MS, electrospray, m/z=583.5 [M+H], RT 1.31 min (MethodB2);

Resolution: Chiralcel OD-H, 20×250 mm 5.8% MeOH (˜1% Et2NH) in CO2 at 85g/min, 160 Bar, 40 C.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 4-23,and other appropriate starting materials and purification conditions:

Compound 216: MS, electrospray, m/z=555.3 [M+H], RT 0.64 min (MethodB1);

Compound 247: MS, electrospray, m/z=557.1 [M+H], RT 1.21 min (MethodB2);

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 146: MS, electrospray, m/z=597.4 [M+H], RT 0.65 min (MethodB1);

Compound 152: MS, electrospray, m/z=597.4 [M+H], RT 0.65 min (MethodB1);

Resolution: Chiralcel OD-H, 20×250 mm 5.8% MeOH (˜1% Et₂NH) in CO₂ at 85g/min, 160 Bar, 40° C.;

Compound 153: MS, electrospray, m/z=597.4 [M+H], RT 0.65 min (MethodB1);

Resolution: Chiralcel OD-H, 20×250 mm 5.8% MeOH (˜1% Et₂NH) in CO₂ at 85g/min, 160 Bar, 40° C.;

Compound 155: MS, electrospray, m/z=613.4 [M+H], RT 0.55 min (MethodB1);

Compound 156: MS, electrospray, m/z=573.4 [M+H], RT 0.43 min (MethodB1);

Compound 163: MS, electrospray, m/z=625.3 [M+H], RT 0.77 min;

Compound 164: MS, electrospray, m/z=555.3 [M+H], RT 0.71 min;

Compound 172: MS, electrospray, m/z=597.3 [M+H], RT 1.31 min (MethodB2);

Compound 179: MS, electrospray, m/z=613.1 [M+H], RT 0.67 min (MethodB1);

Compound 189: MS, electrospray, m/z=583.5 [M+H], RT 0.63 min

Compound 193: MS, electrospray, m/z=583.51 [M+H], RT 0.63 min

Compound 208: MS, electrospray, m/z=587.3 [M+H], RT 1.48 min (MethodB2);

Compound 236: MS, electrospray, m/z=597.3 [M+H], RT 1.54 min (MethodA2);

Resolution: LUX 5 u Cellulose 1 Prep 7% EtOH:Heptane @ 10 ml/min

Compound 238: MS, electrospray, m/z=569.2 [M+H], RT 0.60 min;

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-17, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 135: MS, electrospray, m/z=611.5 [M+H], RT 0.86 min;

Compound 136: MS, electrospray, m/z=611.5 [M+H], RT 0.83 min;

Compound 137: MS, electrospray, m/z=597.5 [M+H], RT 0.84 min;

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-18, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 148: MS, electrospray, m/z=609.4 [M+H], RT 0.81 min;

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-19, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 133: MS, electrospray, m/z=597.5 [M+H], RT 0.81 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-20, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 134: MS, electrospray, m/z=611.5 [M+H], RT 0.85 min;

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-21, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 149: MS, electrospray, m/z=613.3 [M+H], RT 0.74 min;

Compound 150: MS, electrospray, m/z=599.5 [M+H], RT 0.72 min;

Compound 151: MS, electrospray, m/z=613.3 [M+H], RT 0.74 min;

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 4-19,and other appropriate starting materials and purification conditions:

Compound 183: MS, electrospray, m/z=573.1 [M+H], RT 0.53 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 182: MS, electrospray, m/z=585.9 [M+H], RT 0.55 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 4-19,and other appropriate starting materials and purification conditions:

Compound 181: MS, electrospray, m/z=570.7 [M+H], RT 0.61 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 180: MS, electrospray, m/z=583.7 [M+H], RT 0.64 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 4-19,and other appropriate starting materials and purification conditions:

Compound 209: MS, electrospray, m/z=541.4 [M+H], RT 0.52 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-22, bromide, 5-34,and other appropriate starting materials and purification conditions:

Compound 224: MS, electrospray, m/z=556.7 [M+H], RT 0.52 min.

Example 8 Preparation of5-ethoxy-1-(6-{2-[2-(2-fluoro-1-methyl-ethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-3-methyl-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (49)

Amine, 8-42 (2.94 g, 5.74 mmol) is dissolved in methanol (20 mL), THF(20 mL) and water (10 mL). To this solution is added LiOH (0.971 g,40.60 mmol) and the mixture is heated at 50° C. for 2 h. The reaction iscooled to room temperature and concentrated in vacuo. The crude productis purified by reverse phase column chromatography on C18 (using asolvent gradient of 5-95% MeCN/H₂O+0.1% TFA) to provide 60 (2.94 g). MS,electrospray, m/z=485.1 [M+H], RT 0.68 min).

Amino acid 60 (78.0 mg, 0.15 mmol) is combined with 4 Å molecular sieves(20 mg), 1-fluoro-propan-2-one (100 μL), AcOH (25.0 μL), and Na(CN)BH₃(29.2 mg, 0.44 mmol) in MeOH (4 mL). The mixture is stirred at roomtemperature for 30 min and then heated to 50° C. for 12 h. It is thenconcentrated under N₂, triturated with 1:1 MeOH/DMSO, filtered through a0.45 micron syringe filter, and the filtrate is purified by gradientelution (10-100% MeCN/water+0.1% HCO2H) on a Gilson RP-HPLC.Concentrated in vacuo to afford title compound 49 (70.0 mg). MS,electrospray, m/z=545.3 [M+H], RT 0.72 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 8, using appropriate starting materialsand purification conditions

Compound 64: MS, electrospray, m/z=583.4 [M+H], RT 0.70 min;

Compound 65: MS, electrospray, m/z=597.4 [M+H], RT 0.75 min;

Compound 66: MS, electrospray, m/z=597.4 [M+H], RT 0.72 min;

Compound 67: MS, electrospray, m/z=625.5 [M+H], RT 0.78 min;

Compound 68: MS, electrospray, m/z=569.4 [M+H], RT 0.68 min;

Compound 69: MS, electrospray, m/z=583.4 [M+H], RT 0.70 min;

Compound 70: MS, electrospray, m/z=605.4 [M+H], RT 0.71 min;

Compound 71: MS, electrospray, m/z=569.4 [M+H], RT 0.71 min;

Compound 76: MS, electrospray, m/z=597.4 [M+H], RT 0.79 min;

Compound 77: MS, electrospray, m/z=569.4 [M+H], RT 0.69 min;

Compound 78: MS, electrospray, m/z=583.4 [M+H], RT 0.71 min;

Compound 79: MS, electrospray, m/z=597.4 [M+H], RT 0.75 min;

Compound 80: MS, electrospray, m/z=611.4 [M+H], RT 0.74 min;

Compound 94: MS, electrospray, m/z=587.4 [M+H], RT 0.80 min;

Compound 95: MS, electrospray, m/z=597.4 [M+H], RT 0.82 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 8, using phenol, 3-16, bromide, 4-19, andother appropriate starting materials and purification conditions:

Compound 50: MS, electrospray, m/z=505.2 [M+H], RT 0.66 min;

Compound 51: MS, electrospray, m/z=561.3 [M+H], RT 0.70 min;

Compound 54: MS, electrospray, m/z=589.3 [M+H], RT 0.72 min;

Compound 55: MS, electrospray, m/z=575.2 [M+H], RT 0.71 min;

Compound 56: MS, electrospray, m/z=563.3 [M+H], RT 0.74 min;

Compound 57: MS, electrospray, m/z=623.3 [M+H], RT 0.80 min;

Compound 58: MS, electrospray, m/z=563.2 [M+H], RT 0.76 min.

Example 9 Preparation of intermediate3,3-difluoro-cyclobutanecarbaldehyde (9-44)

Dess-Martin periodinane (2.6 g, 6.1 mmol) is added to a mixture of3,3-difluorocyclobutylmethanol, 9-43, (0.5 g, 4.0 mmol) and NaHCO₃ (1.4g, 16.0 mmol) in dichloromethane (10 mL) at room temperature. Theresulting slurry is stirred in the dark for 15 h and then poured into asolution of saturated aqueous NaHCO₃. The resulting mixture is filteredthrough a hydrophobic frit with excess dichloromethane. The organicfiltrate is washed with saturated aqueous Na₂S₂O₅, and then separatedwith another hydrophobic frit. The filtrate is dried over MgSO₄, andthen filtered through a pad of diatomaceous earth using dichloromethane.All but about 5 mL of dichloromethane is removed by short pathdistillation at atmospheric pressure (50° C. bath temperature). Theremaining solution is cooled to −78° C. for 15 min to precipitateresidual periodinane solids. The solvent is removed by syringe andpassed through a 0.45 micron Millipore filter. The filtrate containingthe crude aldehyde 9-44 (˜0.1M in dichloromethane) is used as is withoutfurther purification or concentration.

Example 10 Preparation of1-(6-{2-[2-(3,3-difluoro-cyclobutylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-3-methyl-phenyl}-pyridin-2-yl)-5-isopropoxy-1H-pyrazole-4-carboxylicacid (4)

Amino 7-41 (56.0 mg, 0.11 mmol) is combined whh 4 Å molecular sieves (20mg), 3,3-difluoro-cyclobutanecarboxaldehyde, 9-44, (100 μL, 0.21 mmol),AcOH (20 μL), and Na(CN)BH₃ (20.01 mg, 0.32 mmol) in MeOH (2.0 mL). Themixture is stirred at room temperature for 30 min, and then heated to50° C. for 12 h. The mixture is diluted with THF (1.0 mL) and water (1.0mL). To this is added LiOH (14.68 mg, 0.64 mmol) and the reaction isheated to 50° C. for 2 h. It is then concentrated under N₂, trituratedwith 1:1 MeOH/DMSO, filtered through a 0.45 micron syringe filter, andthe filtrate is purified by gradient elution (10-100% MeCN/water+0.1%HCO2H) on a Gilson RP-HPLC. Concentrated in vacuo to afford titlecompound 4 (40.0 mg). MS, electrospray, m/z=603.4 [M+H], RT 0.78 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 10, using the appropriate amine, otherappropriate starting materials and purification conditions:

Compound 26: MS, electrospray, m/z=575.3 [M+H], RT 0.73 min;

Compound 29: MS, electrospray, m/z=589.3 [M+H], RT 0.77 min;

Compound 82: MS, electrospray, m/z=561.3 [M+H], RT 0.82 min;

Compound 96: MS, electrospray, m/z=589.4 [M+H], RT 0.96 min.

Example 11 Preparation of intermediate2,2-difluoro-cyclopropanecarbaldehyde (10-46)

EDCI (1.4 g, 7.1 mmol) is added to a mixture of N,O-dimethylaminehydrochloride (600 mg, 6.2 mmol) and 2,2-difluorocyclopropane carboxylicacid, 11-45, (580 mg, 4.8 mmol) in dichloromethane (15 mL) at roomtemperature. N,N-Diisopropylethylamine (3.3 mL, 19.0 mmol) is added andthe mixture is stirred for 3 h. A solution of 1N HCl is added, followedby vigorous stirring for 10 min. The organic phase is separated using ahydrophobic fit and applied directly to a 10 g SiO₂ samplet. The crudematerial is purified on a 50 g HP-Sil SNAP cartridge (Biotage) elutingwith 9:1 dichloromethane/MeOH. The solvent is removed from productcontaining fractions via short-path distillation at atmospheric pressure(bath temp of 70° C.) to afford 11-46 (605 mg).

A solution of 11-46, (605 mg, 3.66 mmol) in dichloromethane at −78° C.is treated dropwise with DIBAL-H (4.2 mL, 1.0 M in dichloromethane) andthen is stirred 2.5 h at −78° C. The reaction is quenched by addition ofsaturated aqueous Rochelle salt solution. An equal volume of water isadded and the mixture is warmed to room temperature. The mixture isvigorously stirred for 3 h, followed by separation of the organic phasewith a hydrophobic frit. The dichloromethane is removed by short pathdistillation at atmospheric pressure (bath temp=62° C.) to afford 11-47(389 mg).

Example 12 Preparation of1-(6-{2-[2-(2,2-difluoro-cyclopropylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-3-methyl-phenyl}-pyridin-2-yl)-5-methoxy-1H-pyrazole-4-carboxylicacid (72)

Amine 12-48 (90.0 mg, 0.18 mmol) is combined with 4 Å molecular sieves(20 mg), 2,2-difluoro-cyclopropanecarboxaldehyde, 11-47, (60.0 mg, 0.54mmol), AcOH (20 μL), and Na(CN)BH₃ (34.0 mg, 0.54 mmol) in MeOH (4.0mL). The mixture is stirred at room temperature for 30 min, and thenheated to 50° C. for 12 h. The mixture is diluted with THF (1.0 mL) andwater (1.0 mL). To this is added LiOH (33.00 mg, 1.43 mmol) and thereaction is heated to 50° C. for 2 h. It is then concentrated under N₂,triturated with 1:1 MeOH/DMSO, filtered through a 0.45 micron syringefilter, and the filtrate is purified by gradient elution (10-100%MeOH/water+0.1% HCO₂H) on a Gilson RP-HPLC. Concentrated in vacuo toafford title compound 72 (7.0 mg). MS, electrospray, m/z=561.3 [M+H],Method A2, RT 1.59 min.

Example 13 Preparation of5-methoxy-1-(6-{3-methyl-2-[2-(2,2,2-trifluoro-ethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (11)

2,2,2-Trifluoroethyl triflate, 13-49, (36.0 uL, 0.23 mmol) is added to amixture of intermediate 12-48 (106.0 mg, 0.21 mmol) andN,N-diisopropylethylamine (190 μL, 1.10 mmol) in MeCN (5.0 mL). Themixture is heated to 45° C. for 4 h and then concentrated in vacuo. Theremaining residue is redissolved in 5 mL of THF/MeOH/water (2:2:1) andtreated with LiOH (25.0 mg, 1.10 mmol). The mixture is then heated to50° C. for 2 h prior to removal of the solvents in vacuo. The remainingcrude residue is purified by gradient elution on a 30 g KP-C18 SNAPcartridge (Biotage) using a gradient of 5-95% MeCN/water+0.1% TFA toafford title compound 11 (103 mg). MS, electrospray, m/z=553.2 [M+H],Method A2, RT 1.13 min.

Example 14 Preparation of intermediate1-methyl-5-oxo-pyrrolidine-3-carbaldehyde (14-51)

Alcohol 14-50 (0.20 g, 1.55 mmol) is combined with polystyrene-bound IBXresin (5.81 g) in dichloromethane (20.0 mL) in a sealed 40 mL vial andis rotated end over end for 20 h. The reaction mixture is filtered awayfrom the resin, and the resin is rinsed several times [first withdichloromethane (10 mL), then with a 1:1 dichloromethane/MeOH (20 mL),again with 1:1 dichloromethane/MeOH (20 mL), and finally withdichloromethane (10 mL)]. The combined filtrates are concentrated undera stream of N₂ to yield a mixture of 14-50 and desired product 14-51.

Example 15 Preparation of5-ethoxy-1-(6-{3-methyl-2-[2-(1-methyl-5-oxo-pyrrolidin-3-ylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (97)

Amino acid 60 (40.0 mg, 0.07 mmol) is combined with 4 Å molecular sieves(20 mg), 14-51 (51.0 mg, 0.200 mmol), AcOH (15.0 μL), and Na(CN)BH₃(13.2 mg, 0.20 mmol) in MeOH (2.0 mL). The mixture is stirred at roomtemperature for 30 min and then heated to 50° C. for 12 h. The crude ispurified by reverse phase column chromatography on C18 (using a solventgradient of 5-95% MeCN/H₂O+0.1% TFA) to afford title compound 97 (27.0mg). MS, electrospray, m/z=596.4 [M+H], RT 0.80 min.

Example 16 Preparation of5-ethoxy-1-(6-{3-methyl-2-[2-(tetrahydro-furan-2-ylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (101)

To a mixture of amine 8-42 (100.0 mg, 0.20 mmol) andN,N-diisopropylethylamine (0.10 mL, 0.59 mmol) in DMF (1.00 mL) is added2-bromomethyltetrahydrofuran (8.0 mg, 0.05 mmol) in DMF (0.06 mL). Themixture is irradiated at 100° C. for 10 min and cooled to roomtemperature. Excess bromide (76.0 mg) is added and the reaction isirradiated multiple times and then stirred at room temperature for 24 h.The reaction mixture is filtered and the filtrate is purified by HPLC(using a solvent gradient of 10-95% MeCN/H₂O+0.1% Formic Acid) toprovide 16-52 (6.0 mg).

16-52 (6.0 mg) is diluted with THF (1.0 mL), water (1.0 mL) and MeOH(1.0 mL). To this is added LiOH (5.0 mg) and the reaction is heated to50° C. for 2 h. The reaction mixture is cooled to room temperature,acidified with 4 N HCl in 1,4-dioxane, and filtered. The filtrate ispurified by HPLC (using a solvent gradient of 10-95% MeCN/H₂O+0.1%Formic Acid) to provide title compound 101 (1.0 mg). MS, electrospray,m/z=569.4 [M+H], RT 0.88 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 16, using the appropriate startingmaterials and purification conditions

Compound 138: MS, electrospray, m/z=639.4 [M+H], RT 1.16 min;

Compound 160: MS, electrospray, m/z=563.3 [M+H], RT 0.96 min.

Example 17 Preparation of1-(6-{2-[2-(2-hydroxy-2-methyl-propyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-3-methyl-phenyl}-pyridin-2-yl)-5-methoxy-1H-pyrazole-4-carboxylicacid (33)

Intermediate 12-48 (90.0 mg, 0.18 mmol) is dissolved in MeCN (5.0 mL) towhich is added Cs₂CO₃ (117.9 mg, 0.36 mmo) and chloride 17-53 (29.5 mg,0.27 mmol). The mixture is heated to 50° C. for 10 h. The reaction wascooled, extracted with EtOAc, washed with brine, dried over MgSO₄, andconcentrated. The resulting material is purified by gradient elution ona 30 g KP-C18 SNAP cartridge (Biotage) using a gradient of 15-65%MeCN/water+0.1% TFA to afford the intermediate ester. The ester isdissolved in 5 mL of THF/MeOH/water (2:2:1) and treated with LiOH (25.0mg, 1.10 mmol). The mixture is then heated to 50° C. for 2 h prior toremoval of the solvents in vacuo. The remaining crude residue ispurified by gradient elution on a 30 g KP-C18 SNAP cartridge (Biotage)using a gradient of 15-65% MeCN/water+0.1% TFA to afford title compound33 (103.0 mg). MS, electrospray, m/z=543.2 [M+H], RT 0.68 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 17, using the appropriate startingmaterials and purification conditions

Compound 74: MS, electrospray, m/z=577.3 [M+H], RT 0.67 min;

Compound 168: MS, electrospray, m/z=587.3 [M+H], RT 0.70 min.

Example 18 Preparation of6-Bromomethyl-8-trifluoromethyl-3,4-dihydro-1H-isoquinoline-2-carboxylicacid tert-butyl ester (18-10)

Commercial acid 18.1 (5.0 g, 22.7 mmol) is dissolved in THF (30 mL) atrt. A 1M solution of borane in THF (34.0 mL, 34.0 mmol) is addeddropwise via syringe. The mixture is then heated to 55° C. o/n beforecooling to rt and quenching with water (5 mL). After stirring for 5 min,12 mL of 2N HCl is added and the mixture is stirred 1 h. dichloromethane(50 mL) and water (50 mL) are then added, and the resulting phases areseparated with a hydrophobic frit. The organic layer is further driedover Na₂SO₄, then refiltered. Concentrated in vacuo to affords an oilthat is purified by gradient elution (5-100% EtOAc/heptane) on a 100 gKP-Sil SNAP cartridge (Biotage). Concentration of the product fractionsdelivers intermediate 18.2 (3.2 g)

Thionyl chloride (SOCl₂) (2.3 mL, 31.5 mmol) is added to a solution ofalcohol 18.2 (3.2 g, 15.5 mmol) in dichloromethane (20 mL) under N₂ at−10° C. After 5 min, the cooling bath is removed and the mixture isheated to reflux for 6 h. The resulting solution is cooled to rt andconcentrated in vacuo. The remaining residue is then azeotroped withPhMe (2×10 mL) and then dissolved in DMF (20 mL). Solid NaCN (840 mg,17.1 mmol) is added and the mixture is heated to 45° C. o/n. Uponcooling to rt, the mixture is diluted with water (25 mL), brine (25 mL),and EtOAc (50 mL). The layers are separated, and the organics are driedover Na₂SO₄, filtered, and concentrated in vacuo. Crude product ispurified by gradient elution (5-100% EtOAc/heptane) on a 100 g KP-SilSNAP cartridge (Biotage). Product fractions concentrated in vacuo toafford 18-3 (3.0 g).

A 1M solution of borane in THF (35 mL, 35 mmol) is added dropwise viasyringe to a solution of 18-3 (3.0 g, 13.9 mmol) in THF (25 mL) at rt.The mixture is then heated to 55° C. o/n before cooling to rt, andquenching with water (5 mL). After 5 min of stirring, conc. HCl (8 mL)is added and stirring is continued for 1 h. The mixture is then dilutedwith water (20 mL), and treated with solid NaOH until alkaline.dichloromethane (50 mL) and brine (25 mL) are added, then the layers areseparated with a hydrophobic frit. The crude amine is purified bygradient elution (5-95% MeCN/water+0.1% TFA) on a 120 g KP-C18 SNAPcartridge (Biotage). Concentration of the fractions in in vacuo affordsan intermediate TFA salt (2.93 g) that is dissolved in HCO₂H (30 mL) andtreated with 37% aq. HCHO (0.66 mL, 8.8 mmol). The mixture is stirred at50° C. o/n, then concentrated in vacuo to afford a crude solid that isimmediately dissolved in 48% aq. HBr (25 mL). This solution is heated to100° C. o/n, then concentrated in vacuo. The crude material isazeotroped with PhMe (3×15 mL), then slurried in dichloromethane (50 mL)and DMF (10 mL). Et₃N (1.9 mL, 0.82 mmol) and a few crystals of 4-DMAPare added. Boc₂O (2.0 g, 9.1 mmol) is added in one portion, and themixture is stirred at rt o/n. Saturated NH4Cl solution (50 mL) is addedand the layers are separated with a hydrophobic frit. The organic isconcentrated in vacuo to afford a crude residue that is purified bygradient elution (5-100% EtOAc/heptane) on a 100 g KP-Sil SNAP cartridge(Biotage). Concentration of the product fractions afforded 18-5 (540mg).

Tf₂O (0.27 mL, 1.6 mmol) is added via syringe to a mixture of 18-5 (540mg, 1.46 mmol), Et₃N (0.31 mL, 2.2 mmol) and 4-DMAP (18 mg, 0.15 mmol)in dichloromethane (25 ml) cooled to 0° C. The mixture is stirred withwarming to rt o/n, and then quenched with sat. NaHCO₃ (30 mL). Theresulting layers are separated with a hydrophobic frit, and the organicsare concentrated under N₂. The crude residue is purified by gradientelution (5-30% EtOAc/heptane) on a 50 g HP-Sil SNAP cartridge (Biotage).Concentration of the product fractions in vacuo affords 18-6 (460 mg).

Triflate 18-6 (460 mg, 1.02 mmol) is combined with vinylboronicacid-pyridine complex (250 mg, 1.04 mmol) and Pd(PPh₃)₄ (60 mg, 0.05mmol) in a mixture of DME (9 mL) and 2M aq. Na₂CO₃ solution. The mixtureis irradiated in Biotage microwave at 120° C. for 40 min. Upon cooling,then mixture is concentrated under N₂, and the crude solids andtriturated with dichloromethane. The dichloromethane filtrate is thenpurified by gradient elution (5-80% EtOAc/heptane) using a 50 g HP-SilSNAP cartridge (Biotage). Product fractions concentrated in vacuo toafford 18-7 (275 mg).

Styrene 18-7 (275 mg, 0.84 mmol) and NaIO₄ (630 mg, 2.95 mmol) arecombined in a mixture of THF (12 mL) and water (3 mL) at rt. OsO₄ (0.13mL, 0.017 mmol, 4 wt % in H₂O) is added via syringe and the resultingslurry is stirred vigorously o/n at rt. The slurry is then filteredthrough a frit, and concentrated in vacuo. The remaining residue isdissolved in dichloromethane (20 mL), and washed with saturate aq.thiosulfate solution (25 mL). The layers are then separated with ahydrophobic frit, and the organic concentrated in vacuo. Purification ofthe crude residue by gradient elution (5-60% EtOAc/heptane) on a 25 gHP-Sil SNAP cartridge (Biotage) affords 18-8 (228 mg).

Aldehyde 18-8 (225 mg, 0.683 mmol) is dissolved in THF (5 mL) and thenMeOH (5 mL). Solid NaBH₄ (40 mg, 1.1 mmol) is added, and the mixture isstirred at rt for 20 min. Aqueous sat. NH₄Cl (ca 50 mL) is added and themixture is stirred for 15 min. EtOAc (100 ml) and brine (100 mL) areadded, then the layers are separated. The organic is dried over Na₂SO₄,filtered, and concentrated in vacuo. The crude product is purified bygradient elution (5-100% EtOAc/heptane) on a 50 g HP-Sil SNAP cartridge(Biotage). Concentration of the product fractions in vacuo affords 18-9(225 mg).

Solid Ph₃PBr₂ (450 mg, 1.02 mmol) is added to a mixture of 18-9 (225 mg,0.68 mmol) and DIPEA (0.21 mL, 1.2 mmol) in dichloromethane at 0° C. Themixture is stirred for 1 hour, and then concentrated in vacuo. The crudebromide is purified by gradient elution (5-40% EtOAc/heptanes) on a 25 gHP-SIl SNAP cartridge (Biotage) to afford 18-10 (248 mg).

Similarly, the following bromides were prepared from the appropriatestarting materials as described in Example 18:

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 18-10,and other appropriate starting materials and purification conditions:

Compound 158: MS, electrospray, m/z=623.3 [M+H], RT 1.34 min (MethodB2).

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 18-10,and other appropriate starting materials and purification conditions:

Compound 157: MS, electrospray, m/z=637.3 [M+H], RT 0.67 min (MethodB2).

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 18-11,and other appropriate starting materials and purification conditions:

Compound 201: MS, electrospray, m/z=573.3 [M+H], RT 1.14 min (MethodB2);

Compound 202: MS, electrospray, m/z=589.3 [M+H], RT 1.14 min (MethodB2);

Compound 229: MS, electrospray, m/z=587.3 [M+H], RT 1.46 min (MethodB2);

Resolution: LUX 5 u Cellulose 3 Prep 14% (1:1:1 MeOH:EtOH:iPA):CO₂, 40°C., 110 bar, 80 ml/min

Compound 230: MS, electrospray, m/z=559.3 [M+H], RT 1.46 min (MethodB2).

Resolution: LUX 5 u Cellulose 3 Prep 14% (1:1:1 MeOH:EtOH:iPA):CO₂, 40°C., 110 bar, 80 ml/min

Compound 253: MS, electrospray, m/z=559.4 [M+H], RT 1.20 min (Method A2)(Med Polar Long).

Compound 254: MS, electrospray, m/z=559.3 [M+H], RT 1.20 min (Method A2)(Med Polar Long).

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 18-12,and other appropriate starting materials and purification conditions:

Compound 177: MS, electrospray, m/z=545.2 [M+H], RT 0.68 min (MethodB1);

Compound 187: MS, electrospray, m/z=575.3 [M+H], RT 1.13 min (MethodB2);

Compound 231: MS, electrospray, m/z=589.3 [M+H], RT 1.26 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep 20% 1:1:1 MeOH:EtOH:iPA (0.1%Et₂NH):CO₂ @ 75 ml/min., 130 bar, 40° C.

Compound 234: MS, electrospray, m/z=589.3 [M+H], RT 1.26 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep 20% 1:1:1 MeOH:EtOH:iPA (0.1%Et₂NH):CO₂ @ 75 ml/min., 130 bar, 40° C.

Compound 251: MS, electrospray, m/z=559.4 [M+H], RT 1.18 min (Method A2)(Med Polar Long).

Resolution: ChiralPak AD-H Prep 45% 3:1 hexane:EtOH (1% iPrNH₂):CO₂ @ 80ml/min., 100 bar, 25° C.

Compound 252: MS, electrospray, m/z=559.3 [M+H], RT 1.18 min (Method A2)(Med Polar Long).

Resolution: ChiralPak AD-H Prep 45% 3:1 hexane:EtOH (1% iPrNH₂):CO₂ @ 80ml/min., 100 bar, 25° C.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 18-13,and other appropriate starting materials and purification conditions:

Compound 166: MS, electrospray, m/z=623.3 [M+H], RT 1.30 min (MethodB2).

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 18-12,and other appropriate starting materials and purification conditions:

Compound 159: MS, electrospray, m/z=587.3 [M+H], RT 0.61 min (MethodB1).

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 18-13,and other appropriate starting materials and purification conditions:

Compound 165: MS, electrospray, m/z=637.3 [M+H], RT 1.42 min (MethodB2).

Example 19 Preparation of intermediate7-Hydroxymethyl-6-methyl-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylicacid tert-butyl ester (19-14)

A solution of compound 19-1 (100 g, 0.465 mol) in THF (800.000 ml) isadded to a mixture of LAH (166 g, 1.395 mol) in anhydrous THF (200 ml)at 0° C. The mixture is stirred at room temperature for 0.5 h, then isrefluxed for 1 h. TLC showed the reaction is completed. A saturatedaqueous NH₄Cl (200 ml) is slowly added to the mixture. Then EtOAc andNa₂SO₄ are added. The mixture is stirred for 1 h, and then is filteredand washed by PE to afford compound 19-2.

To a solution of compound 19-2 (360.000 g, 2.365 mol) in dichloromethane(3000.000 ml) is added SOCl₂ (562.980 g, 4.731 mol) at −10° C. Then thereaction mixture is refluxed for 4 h. The mixture is concentrated toafford crude compound 19-3 which is used directly in the next step.

A mixture of compound 19-3 (334.000 g, 1.957 mol) and NaCN (168.096 g,2.290 mol) in DMF (1000.000 ml) is stirred at room temperatureovernight. The mixture is extracted with EtOAc and H₂O. The organiclayer is dried and concentrated, and purified by chromatography onsilica gel (PE:EA=50:1) to give compound 19-4 as a yellow oil.

A mixture of compound 19-4 (1608.000 g, 9.975 mol), KOH (1117.221 g,19.950 mol) in EtOH (15000.000 ml) is heated to reflux for 5 h. TLCshowed the reaction is completed. The solvent is removed under reducedpressure. The residue is adjusted to pH=1. The mixture is filtered andthe filter cake is dried to yield compound 19-5.

Compound 19-5 (737.000 g, 4.090 mol) is added to a stirred solution of(COCl)₂ (8.180 mol) and DMF (70.000 ml) in dichloromethane (7370.000 ml)under N₂ atmosphere, followed by stirring for 2 h. TLC showed thereaction is completed. Then the mixture is evaporated. The residue wasadded to a stirred solution of 2,2-dimethoxyethyl-1-amine (429.996 g,4.090 mol) and Et₃N (454.388 g, 4.499 mol) in dichloromethane (1000 ml)at room temperature for 2 h. TLC showed the reaction is completed. Themixture is evaporated and the residue is purified by column to givecompound 19-6.

A solution of compound 19-6 (1053 g, 3.939 mol) in AcOH (2 L) and HCl (2L) is stirred at room temperature for 16 h. TLC showed the reaction iscompleted. The mixture is evaporated. The residue is crystallized,washed with H₂O and EtOH, and then the solid is filtered and dried togive compound 19-7.

A mixture of Pd/C (4 g) and compound 19-7 (40.000 g, 0.197 mol) in AcOH(2 L) is stirred at room temperature under H₂ for 16 h. LCMS showed thereaction is completed. The mixture is filtered, evaporated, and theresidue is crystallized with EtOH. The solid is filtered and dried togive compound 19-8.

To a stirred solution of compound 19-8 (130.000 g, 0.633 mol) in THF(1300.000 ml) is added BMS (127.000 ml, 1.267 mol) slowly under N₂atmosphere, meanwhile the temperature is maintained below −5° C.,followed by stirring for 16 h. LCMS showed the reaction is completed.The reaction is quenched with conc. HCl and then the mixture is refluxedfor 2 h. The solvent is evaporated and the residue is separated withdichloromethane and H₂O. The aqueous phase is adjusted to pH=9 and thesolid is filtered and dried to give compound 19-9.

A solution of compound 19-9 (220.000 g, 1.150 mol) in 48% HBr aqueous(1800.000 ml) is stirred at 110° C. for 4 h under N₂ atmosphere. LCMSshowed the reaction is completed. The mixture is evaporated to givecrude compound 19-10.

A mixture of compound 19-10 (267.000 g, 1.506 mol), Boc₂O (492.595 g,2.260 mol) and TEA (380.368 g, 3.766 mol) in dichloromethane (2670.000ml) is stirred at room temperature for 2 h. The reaction is monitored byTLC. When compound 19-10 is consumed, the reaction mixture isconcentrated under reduce pressure and the residue was purified bycolumn chromatography to give compound 19-11.

A mixture of compound 19-11 (267.000 g, 0.963 mol) and Tf₂O (271.468 g,0.963 mol) in (2670.000 ml) is stirred at room temperature for 2 h underN₂ atmosphere. TLC showed the reaction is completed. The reactionmixture is concentrated under reduce pressure and the residue ispurified by column to give compound 19-12.

A mixture of compound 19-12 (20.000 g, 0.049 mol), dppp (2.000 g),Pd(OAc)₂ (2.000 g) and TEA (9.868 g, 0.098 mol) in EtOH (400.000 ml) isstirred at 80° C. for 12 h under CO atmosphere. The reaction ismonitored by TLC. When the reaction is completed, the reaction mixtureis concentrated under reduce pressure and the residue is purified bycolumn chromatography to give compound 19-13.

To a stirred solution of compound 19-13 (22.000 g, 0.066 mol) in THF(300.000 ml) is slowly added LAH (2.507 g, 0.066 mol), meanwhile thetemperature is maintained below −40° C. After addition is completed, themixture is stirred at room temperature for 2 h. TLC showed the reactionis completed and the reaction is quenched with H₂O. The solvent isremoved under reduced pressure and the residue is separated withdichloromethane and H₂O, the organic phase is dried over anhydrousNa₂SO₄, and evaporated. The residue was purified by column to givecompound 19-14.

Bromination of the alcohol is performed similarly to that of Example 4to yield intermediate7-Bromomethyl-6-methyl-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylicacid tert-butyl ester 19-15.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 19-15,and other appropriate starting materials and purification conditions:

Compound 176: MS, electrospray, m/z=555.3 [M+H], RT 1.19 min (MethodB2);

Compound 184: MS, electrospray, m/z=583.3 [M+H], RT 1.24 min (MethodB2);

Compound 206: MS, electrospray, m/z=569.3 [M+H], RT 1.26 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep, 20% MeOH:EtOH:IPA (1:1:1) (0.1%Et₂NH) in CO₂ at 705 ml/min, 130 Bar, 40° C.

Compound 207: MS, electrospray, m/z=569.3 [M+H], RT 1.26 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep, 20% MeOH:EtOH:IPA (1:1:1) (0.1%Et₂NH) in CO₂ at 705 ml/min, 130 Bar, 40° C.

Compound 222: MS, electrospray, m/z=583.3 [M+H], RT 1.40 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep, 12% MeOH:IPA (1% Et₂NH) in CO₂ at70 ml/min, 105 Bar, 40° C.

Compound 223: MS, electrospray, m/z=583.4 [M+H], RT 1.42 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep, 12% MeOH:IPA (1% Et₂NH) in CO₂ at70 ml/min, 105 Bar, 40° C.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 19-15,and other appropriate starting materials and purification conditions:

Compound 162: MS, electrospray, m/z=597.3 [M+H], RT 1.34 min (MethodB2);

Compound 175: MS, electrospray, m/z=569.3 [M+H], RT 1.31 min (MethodB2);

Compound 190: MS, electrospray, m/z=597.2 [M+H], RT 0.63 min (MethodB1);

Compound 196: MS, electrospray, m/z=585.3 [M+H], RT 0.67 min (MethodB1);

Compound 203: MS, electrospray, m/z=599.3 [M+H], RT 0.67 min (Method B1)

Resolution: Chirapak AD-H, 20×250 mm; 20% EtOH:Heptane@ 8 mL/min,ambient temp.

Compound 204: MS, electrospray, m/z=599.3 [M+H], RT 0.67 min (Method B1)

Resolution: Chirapak AD-H, 20×250 mm; 20% EtOH:Heptane@ 8 mL/min,ambient temp.

Compound 211: MS, electrospray, m/z=613.3 [M+H], RT 1.43 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep 20% iPA+Et₂NH:Heptane @ 9 ml/min

Compound 212: MS, electrospray, m/z=613.3 [M+H], RT 1.43 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep 20% iPA+Et₂NH:Heptane @ 9 ml/min

Compound 214: MS, electrospray, m/z=611.3 [M+H], RT 1.61 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep 30% iPA:CO₂, 110 bar, 75 ml/min,40° C.

Compound 215: MS, electrospray, m/z=611.3 [M+H], RT 1.61 min (MethodB2);

Resolution: LUX 5 u Cellulose 1 Prep 30% iPA:CO₂, 110 bar, 75 ml/min,40° C.

Compound 225: MS, electrospray, m/z=583.3 [M+H], RT 1.41 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep 20% 1:1:1 MeOH:EtOH:iPA (0.1%Et₂NH):CO₂ @ 75 g/min., 110 bar, 40° C.

Compound 226: MS, electrospray, m/z=583.3 [M+H], RT 1.44 min (MethodB2);

Resolution: ESI Industries CC4 Prep 55% 1:1 hexane:MeOH (3% iPrOH, 0.1%iPrNH₂):CO₂ @ 80 ml/min., 100 bar, 25° C.

Compound 227: MS, electrospray, m/z=583.3 [M+H], RT 1.41 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep 20% 1:1:1 MeOH:EtOH:iPA (0.1%Et₂NH):CO₂ @ 75 g/min., 110 bar, 40° C.

Compound 235: MS, electrospray, m/z=583.3 [M+H], RT 1.41 min (MethodB2);

Resolution: LUX 5 u Cellulose 4 Prep

20% 1:1:1 MeOH:EtOH:iPA (0.1% Et₂NH):CO₂ @ 75 g/min., 110 bar, 40° C.

Compound 228: MS, electrospray, m/z=583.3 [M+H], RT 1.44 min (MethodB2);

Resolution: ESI Industries CC4 Prep 55% 1:1 hexane:MeOH (3% iPrOH, 0.1%iPrNH₂):CO₂ @ 80 ml/min., 100 bar, 25° C.

Compound 232: MS, electrospray, m/z=597.3 [M+H], RT 1.54 min (MethodA2);

Resolution: LUX 5 u Cellulose 1 Prep 7% EtOH:Heptane @ 10 ml/min

Compound 233: MS, electrospray, m/z=597.3 [M+H], RT 1.50 min (MethodA2);

Resolution: LUX 5 u Cellulose 4 Prep 20% EtOH:CO₂, 80 ml/min, 110 bar,40° C.

Compound 235: MS, electrospray, m/z=597.3 [M+H], RT 1.50 min (MethodA2);

Resolution: LUX 5 u Cellulose 4 Prep 20% EtOH:CO₂, 80 ml/min, 110 bar,40° C.

Example 20 Preparation of intermediate5-Bromomethyl-4,7-dimethyl-1,3-dihydro-isoindole-2-carboxylic acidtert-butyl ester (20-4)

To a 100 mL round bottom flask is added amine 20-1 (0.500 g, 4.13 mmol)which is dissolved in dichloromethane (15.0 mL). The reaction mixture iscooled to 0° C. and triethylamine (1.15 mL, 8.25 mmol) and BOC₂O (1.35g, 6.19 mmol) are added. The reaction is warmed to room temperature andstirred overnight. The reaction is extracted with dichloromethane,washed with water and brine, dried over MgSO₄ and concentrated. Theresulting residue is purified by silica gel chromatography using agradient of 12-100% EtOAc in heptanes. The desired fractions arecollected and concentrated yielding an oil (0.556 g).

Propargyl alcohol (0.579 mL, 9.94 mmol) is added dropwise at 0° C. to asolution of diacetylene 20-2 (0.550 g, 2.49 mmol) in anhydrous ethanol(15.0 mL). Wilkinson's catalyst (0.229 g, 0.249 mmol) is added and themixture is stirred for 16 h at room temperature. The crude reaction isconcentrated and subjected to silica gel chromatography using a gradientof 10-80% EtOAc in heptanes. The desired fractions are collected andconcentrated yielding an off-white solid (0.125 g).

To a solution of alcohol 20-3 (125 mg, 0.451 mmol) andN,N-diisopropylethylamine (0.118 mL, 0.676 mmol) in dichloromethane (5.0mL) is added triphenylphosphine dibromide (297 mg, 0.676 mmol) at 0° C.The reaction is stirred for 2 h and concentrated in vacuo. The resultingresidue is purified by silica gel chromatography using a gradient of7-60% EtOAc in heptanes to yield the desired product 20-4 (35.0 mg) as awhite solid.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 20-4, andother appropriate starting materials and purification conditions:

Compound 145: MS, electrospray, m/z=569.3 [M+H], RT 0.75 min;

Compound 246: MS, electrospray, m/z=585.0 [M+H], RT 1.40 min (MethodB2);

Example 21 Preparation of intermediate6-Bromomethyl-5,8-dimethyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester (21-8)

Ketone 21-1 (14.00 g, 70.27 mmol) and pyrrolidine (8.71 mL, 106.0 mmol)are dissolved in toluene (60 mL) and the mixture is refluxed under DeanStark conditions for 24 h. The reaction is then concentrated in vacuo.The resulting residue is dissolved in toluene (60 mL) and treated with4-hexen-3-one (8.32 mL, 70.27 mmol) and hydroquinone (0.080 g, 0.727mmol). The solution is heated to reflux for 24 h and then diluted withEtOAc and washed with 1N HCl. The combined organics are dried andconcentrated in vacuo to afford a viscous oil. The material is purifiedby silica gel chromatography using a gradient of 20-100% EtOAc inheptanes to afford a yellow solid (11.74 g).

A 1.0 M LiHMDS solution (42.95 mL) is added dropwise to a solution ofintermediate 21-2 (10.00 g, 35.79 mmol) in THF (50.0 mL) at −78° C. Thismixture is stirred at −78° C. for an additional 30 min. TMS-Cl (5.45 mL,42.95 mmol) is added dropwise and stirred at −78° C. for 2 h. Thereaction is warmed to room temperature and diluted with diethyl ether(200 mL). This mixture is added to a saturated Na₂CO₃ solution and thephases are separated. The combined organics are dried and concentratedin vacuo. The residue is dissolved in ACN (50.0 mL) and Pd(OAc)₂ (8.04g, 35.79 mmol) is added. The resulting mixture is cooled in a water bathto maintain reaction temp below 35° C. and stirred overnight. Thereaction is filtered through celite and the filtrate is concentrated invacuo. The residue is taken up in 200 mL EtOAc then treated with 1.0 MTBAF solution (50.0 mL). This mixture is stirred for 30 min and thenwashed with 1N HCl and 10% sodium thiosulfate solution. The organics aredried and concentrated. The material is purified by silica gelchromatography using a gradient of 20-80% EtOAc in heptanes to afford anoff-white solid (6.11 g).

To a solution of starting material 21-3 (1.50 g, 5.41 mmol) indichloromethane (25.0 mL) at room temperature is added pyridine (0.871mL, 10.82 mmol). The solution is cooled to −30° C. and Tf₂O (1.00 mL,5.95 mmol) is added dropwise. The reaction is stirred at −30° C. for 1 hand then is warmed to room temperature. It is concentrated in vacuo andthe residue is diluted with EtOAc, washed with 1 N HCl, saturatedNaHCO₃, brine, dried over MgSO₄, and concentrated. The resultingmaterial is purified by silica gel chromatography using a gradient of12-100% EtOAc in heptanes to yield a white solid (1.61 g).

Triflate 21-4 (1.00 g, 2.44 mmol) is combined with the boronate (0.647g, 2.69 mmol) and Pd(PPh₃)₄ (0.144 g, 0.124 mmol) in a mix of DME (15.0mL) and 2.0 M Na₂CO₃ (1.27 mL). The reaction is irradiated in MW at 120°C. for 40 min. It is concentrated under N₂ and is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptanes. Thedesired fractions are concentrated to afford a white solid (0.662 g).

Substrate 21-5 (1.029 g, 3.58 mmol), NaIO₄ (2.34 g, 10.94 mmol), 2.5 wt% OSO₄ in t-BuOH (1.0 mL), THF (12.4 mL) and H₂O (2.4 mL) are combinedat room temperature, then stirred overnight in the dark. The reactionmixture is diluted with water and dichloromethane. The layers areseparated with a hydrophobic frit. The organics are dried over Na₂SO₄,filtered, and concentrated. The residue is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptanes to yield anamber oil (0.786 g).

Aldehyde 21-6 (0.785 g, 2.71 mmol) is dissolved in THF (5.0 mL) and MeOH(5.0 mL). The mixture is cooled to 0° C. and NaBH₄ (0.156 g, 4.07 mmol)is added. The reaction is stirred at room temperature for 30 min. Thereaction is quenched with aq. NH₄Cl and is stirred for 10 min. It isextracted with EtOAc, washed with NH₄Cl, brine, dried over MgSO₄, andconcentrated. The resulting material is purified by silica gelchromatography using a gradient of 12-100% EtOAc in heptanes. Thedesired fractions are collected to yield the desired product 21-7 (0.626g) as a white solid.

To a solution of alcohol 21-7 (0.300 g, 1.030 mmol) andN,N-diisopropylethylamine (0.269 mL, 1.54 mmol) in dichloromethane (10.0mL) is added triphenylphosphine dibromide (0.679 g, 1.54 mmol) at 0° C.The reaction is stirred for 2 h and concentrated in vacuo. The resultingresidue is purified by silica gel chromatography using a gradient of7-60% EtOAc in heptanes to yield the desired product 21-8 (0.338 g) as awhite solid.

Similarly, the following bromides were prepared from the appropriatestarting materials as described in Example 21:

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 21-8, andother appropriate starting materials and purification conditions:

Compound 120: MS, electrospray, m/z=583.5 [M+H], RT 0.74 min;

Compound 178: MS, electrospray, m/z=555.3 [M+H], RT 0.64 min (MethodB1).

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 21-8,and other appropriate starting materials and purification conditions:

Compound 132: MS, electrospray, m/z=597.5 [M+H], RT 0.83 min.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 21-9,and other appropriate starting materials and purification conditions:

Compound 154: MS, electrospray, m/z=597.7 [M+H], RT 0.81 min.

Example 22 Preparation of intermediates5-Bromomethyl-4-methyl-1,3-dihydro-isoindole-2-carboxylic acidtert-butyl ester (22-5) and6-Bromomethyl-4-methyl-1,3-dihydro-isoindole-2-carboxylic acidtert-butyl ester (22-6)

To a stirred solution of Boc-amine 22-1 (2.00 g, 12.89 mmol) in THF(30.0 mL) and tetrabutylammonium iodide (0.476 g, 1.29 mmol) is added0.5 M KHMDS solution (25.8 mL) and the mixture is stirred for 30 min atroom temperature. The bromide (1.69 mL, 19.33 mmol) is added dropwiseand the mixture is stirred for 30 min at room temperature and then isrefluxed for 2 h. The reaction is quenched with saturated NH₄Cl andextracted with EtOAc. The combined organics are dried with MgSO₄ andconcentrated in vacuo. The crude material is purified by silica gelchromatography using a gradient of 5-40% EtOAc in heptanes to yield thedesired product (2.13 g) as a colorless oil.

Propargyl alcohol (2.39 mL, 41.11 mmol) is added dropwise at 0° C. to asolution of diacetylene 22-2 (2.13 g, 10.28 mmol) in anhydrous ethanol(50.0 mL). Wilkinson's catalyst (0.95 g, 1.028 mmol) is added to themixture and it stirred overnight at room temperature. The crude reactionis concentrated in vacuo and subjected to silica gel chromatographyusing a gradient of 10-80% EtOAc in heptanes. The desired fractions arecollected and concentrated to afford both regioisomers 22-3 and 22-4(1.93 g). The mixture is carried on to the next step.

To a solution of the mixture of alcohols 22-3 and 22-4 (1.93 g, 7.33mmol) and N,N-diisopropylethylamine (1.91 mL, 10.98 mmol) indichloromethane (50.0 mL) is added triphenylphosphine dibromide (4.73 g,10.98 mmol) at 0° C. The reaction is stirred for 2 h and concentrated invacuo. The resulting residue is purified by silica gel chromatographyusing a gradient of 7-60% EtOAc in heptanes to yield the mixture ofregioisomers 22-5 and 22-6 (2.12 g) as a white solid.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 22-5, andother appropriate starting materials and purification conditions:

Compound 256: MS, electrospray, m/z=555.4 [M+H], RT 1.13 min (MethodA2);

Compound 257: MS, electrospray, m/z=527.3 [M+H], RT 1.12 min (MethodA2).

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 22-6, andother appropriate starting materials and purification conditions:

Compound 255: MS, electrospray, m/z=555.4 [M+H], RT 1.15 min (MethodA2);

Compound 258: MS, electrospray, m/z=527.3 [M+H], RT 1.16 min (MethodA2).

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 22-5,and other appropriate starting materials and purification conditions:

Compound 119: MS, electrospray, m/z=569.3 [M+H], RT 1.13 min (MethodA2);

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 22-6,and other appropriate starting materials and purification conditions:

Compound 118: MS, electrospray, m/z=569.3 [M+H], RT 1.11 min (MethodA2);

Example 23 Preparation of intermediate5-Bromomethyl-6-methyl-1,3-dihydro-isoindole-2-carboxylic acidtert-butyl ester (23-3)

The alcohol (0.968 mL, 12.94 mmol) is added dropwise at 0° C. to asolution of diacetylene 23-1 (500 mg, 2.59 mmol) in anhydrous ethanol(12.0 mL). Wilkinson's catalyst (239.4 mg, 0.259 mmol) is added to themixture and it stirred overnight at room temperature. The crude reactionis concentrated in vacuo and subjected to silica gel chromatographyusing a gradient of 10-80% EtOAc in heptanes. The desired fractions arecollected and concentrated yielding a solid (105 mg).

To a solution of alcohol 23-2 (105 mg, 0.399 mmol) andN,N-Diisopropylethylamine (0.104 mL, 0.598 mmol) in dichloromethane (7.0mL) is added triphenylphosphine dibromide (263 mg, 0.598 mmol) at 0° C.The reaction is stirred for 2 h and concentrated in vacuo. The resultingresidue is purified by silica gel chromatography using a gradient of7-60% EtOAc in heptanes to yield 23-3.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 23-3, andother appropriate starting materials and purification conditions:

Compound 143: MS, electrospray, m/z=555.4 [M+H], RT 0.74 min.

Example 24 Preparation of5-Ethoxy-1-(6-{3-methyl-2-[5-methyl-2-(tetrahydro-pyran-4-carbonyl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid (Compound 147)

Amine 12-48 (122 mg, 0.232 mmol) is combined with DMAP (2 mg, 0.02 mmol)and DIPEA (60 μL, 0.34 mmol) in dichloromethane (5 mL) at rt.Tetrahydro-2H-pyran-4-carbonyl chloride (40 μL, 0.23 mmol) is added, andthe mixture is stirred overnight at rt. The mixture is applied directlyto a samplet, and then purified by elution with 100% dichloromethane ona 50 g HP-Sil SNAP cartridge (Biotage). Concentration in vacuo affordsthe intermediate ester (31 mg) that is used immediately in the nextstep.

Ester (30 mg) is dissolved in EtOH/H₂O/THF (1, 0.5, 0.5 mL) and treatedwith LiOH (26 mg, 1.2 mmol). The mixture is stirred at 45° C. o/n, andthen concentrated under N₂. The residue is then purified by gradientelution (5-95% MeCN/water+0.1% TFA) on a 12 g KP-C18 SNAP cartridge(Biotage). The product is concentrated in vacuo, to afford Compound 150(26 mg).

Compound 147: MS, electrospray, m/z=611.3 [M+H], RT 1.04 min (Method B1)

Example 25 Preparation of intermediate6-Bromomethyl-8-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester (25-14)

To a mixture of 25-01 (185 g; 0.940 mol), K₂CO₃ (437 g, 3.17 mol) inacetone (2 L) is added MeI (424 g, 2.99 mol). The mixture is stirred at40° C. for 16 h. After filtration, the mixture is purified by silica gelcolumn (PE:EtOAc=500:1) to give 1-Bromo-3-methoxy-5-methyl-benzene,25-02 (189 g) as a light yellow oil.

To a mixture of 25-02 (200 g, 0.995 mol) in dry THF (1.70 L) is addeddropwise n-BuLi (438 ml; 1.09 mol) at −70° C. After stirring for 1 h at−70° C., dry DMF (76.3 g, 1.04 mol) is added dropwise at −70° C. andstirred for 1 h at −70° C. The mixture is poured into NH₄Cl (1.00 L) andextracted with EtOAc (500 mL×3), washed with brine (500 mL×2), driedover Na₂SO₄ and concentrated to give 3-Methoxy-5-methylbenzaldehyde,25-03 (147 g) as a yellow oil.

The mixture of 25-03 (150 g, 0.999 mol) and NH₄OAc (30.8 g, 0.40 mol) inMeNO₂ (1.5 L) is refluxed for 16 h. The mixture is concentrated, thendiluted with EtOAc (1000 mL), washed with water (1 L), brine (100 mL),the organic layers are dried over Na₂SO₄ and concentrated. The mixtureis triturated with PE:EtOAc=10:1 for 10 minutes, filtered to give1-Methoxy-3-methyl-5-((E)-2-nitro-vinyl)-benzene, 25-04 (80 g) as yellowsolid.

To a mixture of LiAlH₄ (78.6 g, 2.00 mol) in dry THF (1 L) is added25-04 (78 g, 0.404 mol) in portions at 0° C. in THF (200 mL) and stirredfor 16 h at 70° C. The mixture is cooled to 0° C., quenched slowly withwater (78 mL), 15% NaOH (78 mL) and water (235 mL). After filtration,the mixture is concentrated to give2-(3-Methoxy-5-methyl-phenyl)-ethylamine, 25-05 (40 g) as a light yellowoil.

The mixture of compound 25-05 (66 g, 0.40 mol) and formic acid (73.5 g,1.60 mol) in dioxane (600 mL) is stirred for 16 h at 90° C. The mixturewas concentrated to giveN-[2-(3-Methoxy-5-methyl-phenyl)-ethyl]-formamide, 25-06 (77 g) asyellow solid.

To a solution of 25-06 (76.0 g, 0.354 mol) in dichloromethane (2.5 L) isadded POCl₃ (155 g, 1.01 mol) at 15° C. and refluxed for 3 h. Thesolution is concentrated, to the residue is added water (1.5 L), toluene(1.5 L) and 20% NaOH (500 mL), then refluxed for 1 h and cooled. Themixture is diluted with EtOAc (500 mL×3), washed with water (1 L×2),brine (100 mL×2), the combined organics were dried over Na₂SO₄ andconcentrated. It is purified by silica gel column (PE:EtOAc=10:1) togive 6-Methoxy-8-methyl-3,4-dihydroisoquinoline, 25-07 (58.5 g) as brownoil.

To a solution of 25-07 (58.5 g, 0.334 mol) in MeOH (500 mL) is addedNaBH₄ (63.3 g, 1.67 mol) at 0° C. and the mixture is maintained at 0° C.for 4 h. The solution is quenched with 1N HCl (100 mL), pH is adjustedto 8 by addition of NaHCO₃, extracted with dichloromethane (300 mL×2),the combined organics are dried over Na₂SO₄ and concentrated to afford6-Methoxy-8-methyl-3,4-dihydro-isoquinoline, 25-08 (83 g, crude) asbrown oil.

A solution of crude 25-08 (83 g, 0.47 mol) in HBr (40% in water, 500 mL)is heated to 90° C. for 12 h. The solution is evaporated under reducedpressure to obtain 8-Methyl-1,2,3,4-tetrahydro-isoquinolin-6-olhydrobromide, 25-09. To this crude residue is added Boc₂O (72 g, 0.33mol) and triethylamine (63 g, 0.62 mol) and the resulting mixture isstirred for 12 h at 15° C., then diluted with dichloromethane (1500 mL)and water (100 mL). The organics layer is washed with 0.5 N HCl (100 mL)and brine (100 mL), dried, concentrated, and purified by silica gelcolumn (PE:EtOAc=30:1) to give6-Hydroxy-8-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester, 25-10 (33.4 g) as a white solid.

To a solution of 25-10 (33 g; 0.113 mol) and pyridine (20.1 g, 0.254mol) in dry dichloromethane (300 mL) is added Tf₂O (39.4 g, 0.139 mol)drop-wise at −30° C. and stirred for 1 h at −30° C. Then the solution iswarmed to 15° C. and stirred for 8 h. The mixture is diluted withdichloromethane (500 mL) and water (100 mL), and the combined organicsare concentrated and then purified by silica gel column (PE:EtOAc=50:1)to give8-Methyl-6-trifluoromethanesulfonyloxy-3,4-dihydro-1H-isoquinoline-2-carboxylicacid tert-butyl ester, 25-11 (43 g) as a white solid.

A solution of 25-11 (43 g, 0.109 mol), Et₃N (33.0 g, 0.327 mol), DPPP(4.53 g) and Pd(OAc)₂ (5 g) in MeOH (500 mL) is stirred under 3 MPapressure of CO at 90° C. for 2 days. After filtration and concentrationthe residue is purified by silica gel chromatography (PE:EtOAc=50:1) toafford 8-Methyl-3,4-dihydro-1H-isoquinoline-2,6-dicarboxylic acid2-tert-butyl ester 6-methyl ester, 25-12 (21 g) as a colorless oil.

To a solution of 25-12 (21 g, 0.693 mol) in dry THF (500 mL) is addedLiAlH₄ (7.4 g, 208 mmol) at −50° C. The mixture is stirred at −50° C.for 1 h, and then 0° C. for 30 min. The reaction is slowly quenched withH₂O (7.4 mL), 15% NaOH (7.4 mL), and H₂O (22.2 mL) and then filtered.The filtrate is concentrated and purified by prep-HPLC and concentrated.The residue is extracted with dichloromethane (1 L×2), the combinedorganics were dried over Na₂SO₄ and concentrated to give6-Hydroxymethyl-8-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester, 25-13 (14.8 g) as a colorless oil.

To a solution of 25-13 (13.4 g, 0.485 mol) and DIEA (11.8 mL, 0.679 mol)in dichloromethane (200 mL) at −30° C. is added triphenylphosphinedibromide (26.6 g, 0.606 mol). The resulting mixture was stirred 1 h,over which time cold bath is allowed to warm to −10° C. Volatiles arestripped from the −10° C. mixture, the residue is suspended indichloromethane (50 mL), and the filtrate is purified by chromatography(silica gel, 5-40% EtOAc in heptane) to provide the desired intermediate25-14 (16.2 g) as a white solid.

Similarly, the following bromides were prepared from the appropriatestarting materials as described in Example 25:

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 1-6, bromide, 25-14,and other appropriate starting materials and purification conditions:

Compound 161: MS, electrospray, m/z=597.3 [M+H], RT 0.75 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 25-14,and other appropriate starting materials and purification conditions:

Compound 171: MS, electrospray, m/z=569.3 [M+H], RT 0.68 min;

Compound 186: MS, electrospray, m/z=541.3 [M+H], RT 0.60 min;

Compound 237: MS, electrospray, m/z=569.3 [M+H], RT 0.60 min;

Compound 239: MS, electrospray, m/z=569.3 [M+H], RT 0.60 min;

Compound 240: MS, electrospray, m/z=585.2 [M+H], RT 0.60 min;

Compound 242: MS, electrospray, m/z=555.3 [M+H], RT 0.59 min;

Compound 244: MS, electrospray, m/z=557.3 [M+H], RT 0.62 min.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 25-14,and other appropriate starting materials and purification conditions:

Compound 169: MS, electrospray, m/z=583.3 [M+H], RT 0.73 min;

Compound 173: MS, electrospray, m/z=583.3 [M+H], RT 0.74 min;

Compound 174: MS, electrospray, m/z=555.3 [M+H], RT 0.72 min;

Compound 195: MS, electrospray, m/z=583.4 [M+H], RT 0.71 min;

Resolution: IC column 15% 1:1:1 MeOH:EtOH:iPA+diethylamine:CO2, 3ml/min, 40° C., 200 bar

Compound 197: MS, electrospray, m/z=583.4 [M+H], RT 0.71 min;

Resolution: IC column 15% 1:1:1 MeOH:EtOH:iPA+diethylamine:CO2, 3ml/min, 40° C., 200 bar

Compound 200: MS, electrospray, m/z=583.3 [M+H], RT 0.63 min (MethodB1);

Compound 210: MS, electrospray, m/z=571.1 [M+H], RT 0.70 min (MethodB1);

Compound 241: MS, electrospray, m/z=569.3 [M+H], RT 0.62 min;

Compound 243: MS, electrospray, m/z=599.3 [M+H], RT 0.63 min;

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 25-15,and other appropriate starting materials and purification conditions:

Compound 121: MS, electrospray, m/z=569.4 [M+H], RT 0.72 min.

Example 26 Preparation of intermediate6-Bromomethyl-8-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester (26-12)

A round-bottom flask is charged with 2-Hydroxy-4-iodobenzoic acid methylester, 26-01 (12.0 g, 43.2 mmol),2,4,6-Trivinyl-cyclotriboroxane-pyridine complex (11.4 g, 47.5 mmol),tetrakis(triphenylphosphine) palladium (2.49 g, 2.16 mmol), 2.0 Maqueous solution of sodium carbonate (25.9 mL, 51.7 mmol), and1,2-dimethoxyethane (50 mL), deoxygenated by alternating between vacuumand argon (3×), and refluxed under argon pressure for 3 h, and thenstirred 18 h at ambient temperature. Volatiles are stripped in vacuo,the residue is suspended in 1N HCl (800 mL) and extracted with EtOAc(600 mL, 300 mL, and then 300 mL). The combined organic extracts arewashed brine, dried over NaSO₄, and purified by chromatography (silicagel, 5-30% EtOAc in heptane) to afford 2-Hydroxy-4-vinyl-benzoic acid,26-02 (3.70 g) and 2-Hydroxy-4-vinyl-benzoic acid methyl ester (0.300g).

To a solution of 26-02 (3.70 g, 22.0 mmol) and 2-Hydroxy-4-vinyl-benzoicacid methyl ester (0.300 g, 1.69 mmol) in MeOH (50 mL) is added H2SO4(4.0 mL, 75 mmol). The resulting mixture is refluxed for 16 h and thenallowed to cool to room temperature. Ice (100 g) is added and themixture is stirred. When the ice completely melts, the MeOH is removedunder reduced pressure and the aqueous residue is extracted with DCM(2×100 mL). The combined organic extracts are combined, concentrated invacuo and purified by chromatography (silica gel, 0-5% EtOAc in heptane)to give 2-Hydroxy-4-vinyl-benzoic acid methyl ester, 26-03 (3.75 g) as aclear oil.

To a stirring mixture of 26-03 (3.75 g, 21 mmol) and Sodiummetaperiodate (13.8 g, 64.3 mmol) in THF (80 mL) and water (20 mL) isadded a 4 wt % solution of osmium tetraoxide in water (3.69 mL, 0.47mmol). The reaction flask (which warms upon addition of the osmiumreagent) is wrapped in aluminum foil to shield contents from light, andthe slurry is stirred 16 h. Volatiles are removed under reducedpressure, the residue is diluted with saturated aqueous NaHCO3 (700 mL)and extracted with EtOAc (700 mL, 200 mL, and then 200 mL). Combinedorganic extracts are concentrated in vacuo and then purified bychromatography (silica gel, 0-50% EtOAc in heptane) to afford4-Formyl-2-hydroxy-benzoic acid methyl ester, 26-04 (2.25 g) as a yellowsolid.

In a round-bottom flask with Dean Stark trap attached, 26-04 (2.25 g, 12mmol) and amino acetaldehyde dimethyl acetal (1.31 g, 12 mmol) arerefluxed in toluene 3 h. Reaction mixture is concentrated in vacuo toafford crude 4-{[2,2-Dimethoxy-ethylimino]-methyl}-2-hydroxy-benzoicacid methyl ester, 26-05 (3.33 g, 12.4 mmol) as a brown oil. To thiscrude oil is added a large stir bar, polyphosphoric acid (25.0 g), andphosphorous pentoxide (33.0 g, 232 mmol). The resulting, viscous tar isstirred at 80° C. for 5 h. The reaction mixture is diluted with H₂O (600mL), transferred to a 5 L Erlenmyer flask, and the vigorously stirredmixture is carefully treated with small portions of solid NaHCO3 untilsaid addition no longer cause receiving mixture to foam. Basic aqueousmixture is then extracted with DCM (5×200 mL). The combined organicextracts are washed with H₂O (2×50 mL), dried with Na2SO4, concentratedunder vacuo and then purified by choratography (silica gel, 0-100% EtOAcin heptane) to yield 5-Hydroxy-isoquinoline-6-carboxylic acid methylester, 26-06 (0.520 g).

26-06 (0.520 g, 2.46 mmol) is dissolved in MeOH (15 mL) and then 4N HClin dioxane (6.15 mL, 24 mmol) is added. Hydrogenated on an H-Cubeapparatus by continuously cycling solution through a PtO₂ cartridge at arate of 1 mL/minute under 10 mbar of H₂-pressure for 5 h, then under 50mbar H₂-pressure for 15 h. Reaction mixture is concentrated underreduced pressure to get crude5-Hydroxy-1,2,3,4-tetrahydro-isoquinoline-6-carboxylic acid methylester; hydrochloride, 26-07 (0.90 g) as a red solid. This crude solid isdissolved in DCM (30 mL) and cooled to 0° C. before adding triethylamine(1.65 mL, 11 mmol) and then di-tert-butyl dicarbonate (1.70 mL, 7.39mmol). Reaction mixture is removed from cold bath, stirred 16 h,concentrated under reduced pressure and purified by chromatography(silica gel, 0-50% EtOAc in heptane). Desired intermediate5-Hydroxy-3,4-dihydro-1H-isoquinoline-2,6-dicarboxylic acid 2-tert-butylester 6-methyl ester 26-08 (0.492 g) co-elutes with di-tert-butyldicarbonate (1.61 g). The mixture (2.1 g) is dissolved in MeOH (50 mL),K₂CO₃ (2.21 g, 16 mmol) is added and the resulting mixture is stirred 16h. Supernatant is removed from reaction flask and sediment is trituratedwith MeOH (2×10 mL). The combined methanolic supernatants areconcentrated under reduced pressure, dissolved in EtOAc (50 mL), washedwith 1N HCl (3×30 mL), brine (10 mL), dried with Na2SO4, andconcentrated in vacuo to get 26-08 (0.422 g). This residue is combinedwith iodomethane (1.0 mL, 16 mmol), K₂CO₃ (0.20 g, 1.5 mmol), Cs₂CO₃(0.40 g, 1.5 mmol), and acetone (4.0 mL) and irradiated in microwave at70° C. for 7 h. Mixture is concentrated under reduced pressure andpurified by chromatography (silica gel, 0-100% EtOAc) to afford impure5-Methoxy-3,4-dihydro-1H-isoquinoline-2,6-dicarboxylic acid 2-tert-butylester 6-methyl ester, 26-09 (0.245 g) which was carried forward as is.

Impure 26-09 (0.240 g, 0.51 mmol) is combined with lithium hydroxide(1.22 g, 5.1 mmol) in THF (4.0 mL), MeOH (4.0 mL) and water (2.0 mL).The mixture is heated 45 minutes at 55° C. and then concentrated underreduced pressure. The residue is dissolved in EtOAc (20 mL), washed with1N HCl (3×50 mL), brine (10 mL), dried with Na₂SO₄, and concentrated invacuo to give crude5-Methoxy-3,4-dihydro-1H-isoquinoline-2,6-dicarboxylic acid 2-tert-butylester, 26-10 (0.177 g) as a white solid.

To a solution of crude 26-10 (0.177 g, 0.58 mmol) in THF (3 mL) is addeda 1M borane in THF solution (1.27 mL, 1.27 mmol) and the resultingmixture is stirred for 18 h. Reaction mixture is concentrated in vacuoand purified by reverse-phase chromatography (C18 silica gel, 5-95%MeCN, in H2O with 0.1% TFA) to get6-Hydroxymethyl-5-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester, 26-11 (0.125 g) as a clear, colorless residue.

26-11 (0.125 g, 0.43 mmol) and N,N-diisopropylethylamine (0.111 mL, 0.64mmol) are dissolved in DCM (4.0 mL), the resulting mixture isdeoxygenated by alternating between argon and vacuum (3×), and thencooled to −30° C. Triphenylphosphine dibromide (0.262 g, 0.60 mmol) isadded and the resulting mixture stirs for 3 h as cold bath warms to −15°C. Reaction mixture is concentrated under reduced pressure and theresidue is purified by chromatography (silica gel, 5-50% EtOAc inheptane) to afford desired intermediate6-Bromomethyl-5-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acidtert-butyl ester, 26-12 (0.103 g).

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 3-15, bromide, 26-12,and other appropriate starting materials and purification conditions:

Compound 220: MS, electrospray, m/z=599.3 [M+H], RT 0.71 min;

Compound 221: MS, electrospray, m/z=571.3 [M+H], RT 0.71 min;

Example 275-Methoxy-1-(6-{3-methyl-2-[5-methyl-1-oxo-2-(tetrahydro-pyran-4-yl)-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy]-phenyl}-pyridin-2-yl)-1H-pyrazole-4-carboxylicacid

To a suspension of compound 27 (0.065 g, 0.11 mmol) in a 4:1 mixture of1,1,2,2,-tetrachloroethane:water (1.2 mL) is added sodium chlorite(0.035 g, 0.39 mmol). The mixture was heated at 55° C. for 2 hours thencooled to room temperature and the mixture purified by C18 flash reversephase chromatography to afford the title compound (0.009 g).

Compound 167: MS, electrospray, m/z=584.8 [M+H], RT 1.01 min.

The following compound is prepared according to the above procedureusing Compound 114 as the appropriate starting materials andpurification conditions:

Compound 194: MS, electrospray, m/z=597.22 [M+H], RT 1.02 min.

Example 28 Preparation of1-{6-[2-(2-(S)-1-[1,4]Dioxan-2-ylmethyl-5-methyl-1,2,3,4-tetrahydro-isoquinolin-6-ylmethoxy)-3-methyl-phenyl]-pyridin-2-yl}-5-ethoxy-1H-pyrazole-4-carboxylicacid

Amine 8-42 (80.0 mg, 0.152 mmol) is dissolved in acetonitrile (3.0 mL)and chloride (16.87 mg, 0.182 mmol) and Cs₂CO₃ (51.5 mg, 0.243 mmol) areadded. The reaction is heated to 60° C. and stirred overnight. LC-MSindicated the desired mass. The reaction is extracted with EtOAc, washedwith brine, dried over MgSO₄, and concentrated. The resulting residue issubjected to silica gel chromatography using a gradient of 12-100% EtOAcin heptanes. The desired fractions are collected and concentrated toyield the product (43.0 mg).

To a solution of epoxide 28-1 (43.0 mg, 0.074 mmol) and DCE (2.0 mL) isadded 2-chloroethanol (0.005 mL, 0.081 mmol) followed by a solution ofBF₃Et₂O (0.01 mL) in DCE. The reaction is stirred at 45° C. overnight.The reaction mixture is cooled to room temperature and is concentrated.The resulting material is carried on crude to the next step.

To starting material 28-2 (40.0 mg) is added a solution of 2.0 M NaOH(2.0 mL). This solution is heated to 90° C. and becomes homogeneous. Itis stirred for 3 h and the reaction is cooled to room temperature. It issubjected to a C18 column (20-80% ACN in Water with 0.1% TFA). Thedesired fractions were collected and concentrated to yield the desiredcompound 18 (19.1 mg).

Compound 185: MS, electrospray, m/z=599.3 [M+H], RT 0.75 min, Method B1.

The following compound is prepared according to the procedure describedin Example 28, using the appropriate starting materials and purificationconditions:

Compound 170: MS, electrospray, m/z=599.3 [M+H], RT 0.63 min, Method B1.

Example 29 tert-Butyl8-ethyl-6(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate(29-13)

To the mixture of compound 29-1 (300 g, 1.6 mol) and K₂CO₃ (665 g, 4.8mol) in DMF (2000 mL) was added MeI (250 g, 1.8 mol) dropwised at roomtemperature. The mixture was stirred overnight. TLC showed the reactionis completed. The reaction was quenched by H₂O and extracted with EtOAc.The organic layer was dried, filtered, evaporated under reduced pressureto give the crude product which was purified by chromatography on silicagel to give compound 29-2 (165 g, 52% yield).

The solution of compound 29-2 (100 g, 497.4 mmol), NBS (88.5 g, 497.4mmol) and AIBN (10 g, 10%) in CCl₄ (700 mL) was heated to reflux for 12h. TLC showed the reaction is completed.

After cooling down to room temperature, the reaction was quenched by H₂Oand extracted with EtOAc. The organic layer was dried, filtered andevaporated under reduced pressure to give the crude product which waspurified by chromatography on silica gel to give compound 29-3 (48 g,42% yield).

The solution of compound 29-3 (80 g, 285.7 mmol) and TMSCN (28.2 g,285.7 mmol) in ACN (600 ml) was stirred at room temperature for 0.5 h.TBAF (74.6 g, 285.7 mmol) was added into the reaction mixture at icebased and the mixture was stirred for 12 h. TLC showed the reaction wascompleted. The reaction was quenched by H₂O and extracted with EtOAc.The organic layer was dried, filtered and evaporated under reducedpressure to give the crude product which was purified by chromatographyon silica gel to give compound 29-4 (39 g, 60% yield).

The solution of compound 29-4 (12 g, 53.1 mmol) and Ni (10 g) in MeOH(80 ml) and NH₃.H₂O (80 ml) was stirred under H₂ with a pressure of 50psi at room temperature for 5 h. TLC showed the reaction was completed.The mixture was filtered and the filtrate was concentrate on vacuum pumpto give the crude product (8 g) which was used directly in the nextstep.

The solution of compound 29-5 (75 g, 326.08 mmol) and HCHO (8.8 g,293.47 mmol) in HCO₂H (500 ml) was stirred at 50° C. under N₂ overnight.LCMS showed the reaction was completed. The solvent was removed underreduced pressure to give the crude product which was purified bychromatography on silica gel to give compound 29-6 (54 g, 64% yield for2 steps).

The solution of compound 29-6 (45 g, 186 mmol) in aqueous HBr solution(400 ml) was stirred at 90° C. for 12 h. LCMS showed the reaction wascompleted. The solvent was removed under reduced pressure to give thecrude product which was purified by chromatography on silica gel to givecompound 29-7 (20.75 g, 53% yield).

The solution of compound 29-7 (20 g, 87.7 mmol), Boc₂O (19.1 g, 87.7mmol) and TEA (17.7 g, 175.4 mmol) in THF/H₂O (1:1) (200 ml) was stirredat room temperature for 3 h. TLC showed the reaction is completed. Thereaction was quenched by H₂O and extracted with EtOAc. The organic layerwas dried, filtered and evaporated under reduced pressure to give thecrude product which was purified by chromatography on silica gel to givecompound 29-8 (20 g, 70% yield).

The solution of compound 29-8 (14 g, 42.7 mmol), K₂CO₃ (17.66 g, 128mmol), Pd(dppf)Cl₂ (2.5 g), Pd (PPh₃)₄ (2.5 g), and compound 29-8B (7.22g, 46.9 mmol) in DMF (150 ml) was stirred at reflux overnight. TLCshowed the reaction is completed. After filtration, the filtrate wasconcentrate under reduced pressure and the residue was purified bychromatography on silica gel to give compound 29-9 (7.2 g, 61% yield).

The solution of compound 29-9 (7.2 g, 26.2 mmol) and Pd—C (2 g) in MeOH(100 ml) was stirred under H₂ with a pressure of 50 psi at roomtemperature for 12 h. TLC showed the reaction was completed. The mixturewas filtered and the filtrate was concentrated to give crude productwhich was purified by chromatography on silica gel to give compound29-10 (5.8 g, 80% yield).

The solution of compound 29-10 (5.8 g, 20.9 mmol), Tf₂O (5.9 g, 20.9mmol) and TEA (6.3 g, 62.7 mmol) in DCM (70 ml) was stirred at roomtemperature for 3 h. TLC showed the reaction was completed. The reactionwas quenched by H₂O and extracted with EtOAc. The organic layer wasdried, filtered and evaporated under reduced pressure to give the crudeproduct which was purified by chromatography on silica gel to givecompound 29-11 (7 g, 82% yield).

A mixture of compound 29-11 (7 g, 17.1 mmol), Pd(OAc)₂ (1.4 g), dppp(1.4 g) and Et₃N (5.2 g, 51.3 mmol) in MeOH (80 mL) was stirred at 80°C. under CO with a pressure of 3 MPa for 2 d. The solid was filtered offand the filtrate was concentrated under reduced pressure. The residuewas purified by chromatography on silica gel to give compound 29-12 (4.8g, 88% yield).

To a solution of LiAlH₄ (1.1 g, 30.1 mmol) in THF (10 mL) was addeddropwise the solution of compound 29-12 (4.8 g, 15.0 mmol) in THF (50mL) at −50° C. over 30 min. After addition, the reaction mixture wasstirred at 0° C. for 2.5 h. Then the reaction mixture was treated withH₂O and DCM. The organic layer was separated, washed with brine, driedover Na₂SO₄, filtered and concentrated under reduced pressure. Theresidue was purified by chromatography on silica gel to give 29-13 (4.1g, 92% yield).

Similarly, the bromide was prepared from 29-13 as described in Example25 producing compound 29-14.

The following compounds from Table 1 are prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 29-14,and other appropriate starting materials and purification conditions:

Compound 248: MS, electrospray, m/z=583.3 [M+H], RT 1.29 min (MethodA2);

Compound 249: MS, electrospray, m/z=555.3 [M+H], RT 1.37 min (MethodA2).

Example 30 tert-Butyl8-cyano-6-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate(30-12)

To the mixture of compound 30-1 (300 g, 1.6 mol) and K₂CO₃ (665 g, 4.8mol) in DMF (2000 mL) was added MeI (250 g, 1.8 mol) dropwised at roomtemperature. The mixture was stirred overnight. TLC showed the reactionis completed. The reaction was quenched by H₂O and extracted with EtOAc.The organic layer was dried, filtered, evaporated under reduced pressureto give the crude product which was purified by chromatography on silicagel to give compound 30-2 (165 g, 52% yield).

The solution of compound 30-2 (100 g, 497.4 mmol), NBS (88.5 g, 497.4mmol) and AIBN (10 g, 10%) in CCl₄ (700 mL) was heated to reflux for 12h. TLC showed the reaction is completed. After cooling down to roomtemperature, the reaction was quenched by H₂O and extracted with EtOAc.The organic layer was dried, filtered and evaporated under reducedpressure to give the crude product which was purified by chromatographyon silica gel to give compound 30-3 (48 g, 42% yield).

The solution of compound 30-3 (80 g, 285.7 mmol) and TMSCN (28.2 g,285.7 mmol) in ACN (600 ml) was stirred at room temperature for 0.5 h.TBAF (74.6 g, 285.7 mmol) was added into the reaction mixture at icebased and the mixture was stirred for 12 h. TLC showed the reaction wascompleted. The reaction was quenched by H₂O and extracted with EtOAc.The organic layer was dried, filtered and evaporated under reducedpressure to give the crude product which was purified by chromatographyon silica gel to give compound 30-4 (39 g, 60% yield).

The solution of compound 30-4 (12 g, 53.1 mmol) and Ni (10 g) in MeOH(80 ml) and NH₃.H₂O (80 ml) was stirred under H₂ with a pressure of 50psi at room temperature for 5 h. TLC showed the reaction was completed.The mixture was filtered and the filtrate was concentrate on vacuum pumpto give the crude product (8 g) which was used directly in the nextstep.

The solution of compound 30-5 (75 g, 326.08 mmol) and HCHO (8.8 g,293.47 mmol) in HCO₂H (500 ml) was stirred at 50° C. under N₂ overnight.LCMS showed the reaction was completed. The solvent was removed underreduced pressure to give the crude product which was purified bychromatography on silica gel to give compound 30-6 (54 g, 64% yield for2 steps).

The solution of compound 30-6 (45 g, 186 mmol) in aqueous HBr solution(400 ml) was stirred at 90° C. for 12 h. LCMS showed the reaction wascompleted. The solvent was removed under reduced pressure to give thecrude product which was purified by chromatography on silica gel to givecompound 30-7 (20.75 g, 53% yield).

The solution of compound 30-7 (20 g, 87.7 mmol), Boc₂O (19.1 g, 87.7mmol) and TEA (17.7 g, 175.4 mmol) in THF/H₂O (1:1) (200 ml) was stirredat room temperature for 3 h. TLC showed the reaction is completed. Thereaction was quenched by H₂O and extracted with EtOAc. The organic layerwas dried, filtered and evaporated under reduced pressure to give thecrude product which was purified by chromatography on silica gel to givecompound 30-8 (20 g, 70% yield).

A solution of compound 30-8 (11 g, 34.8 mmol), Pd(dppf) Cl₂ (2.5 g), Pd(PPh₃)₄ (2.5 g), ZnCN (2.8 g, 31.3 mmol), Zn (1.1 g, 17.4 mmol) in DMF(110 ml) was stirred at reflux overnight. TLC showed the reaction wascompleted. After filtration, the filtrate was concentrate under reducedpressure and the residue was purified by chromatography on silica gel togive compound 30-9 (6.5 g, 71% yield).

The solution of compound 30-9 (12 g, 43.7 mmol), Tf₂O (12.3 g, 43.7mmol) and TEA (13.3 g, 131.23 mmol) in DCM (120 ml) was stirred at roomtemperature for 3 h. TLC showed the reaction was completed. The reactionwas quenched by H₂O and extracted with EtOAc. The organic layer wasdried, filtered and evaporated under reduced pressure to give the crudeproduct which was purified by chromatography on silica gel to givecompound 30-10 (9 g, 51% yield).

A mixture of compound 30-10 (9.5 g, 23.4 mmol), Pd(OAc)₂ (1.9 g), dppp(1.9 g) and Et₃N (7.1 g, 70.1 mmol) in MeOH (90 mL) was stirred at 80°C. under CO with a pressure of 3 MPa for 2 d. The solid was filtered offand the filtrate was concentrated under reduced pressure. The residuewas purified by chromatography on silica gel to give compound 30-11 (6g, 80% yield).

To a solution of LiAlH₄ (1.4 g, 37.9 mmol) in THF (10 mL) was addeddropwise the solution of compound 30-11 (6 g, 19.0 mmol) in THF (50 mL)at −50° C. over 30 min. After addition, the reaction mixture was stirredat −20° C. for 4.5 h. Then the reaction mixture was treated with H₂O andDCM. The organic layer was separated, washed with brine, dried overNa₂SO₄, filtered and concentrated under reduced pressure. The residuewas purified by chromatography on silica gel to give 30-12 (4.1 g, 74%yield).

Similarly, the bromide was prepared from 30-12 as described in Example25 producing compound 30-13.

The following compound from Table 1 is prepared according to theprocedure described in Example 7a, using phenol, 2-8, bromide, 30-13,and other appropriate starting materials and purification conditions:

Compound 250: MS, electrospray, m/z=580.2 [M+H], RT 0.61 min.

Assessment of Biological Activity

Cellular Assay

The sGC cellular activator assay is performed in the presence andabsence of 50% human serum (HS) using Chinese hamster ovary cells thathave been stably transfected to express the human soluble guanylatecyclase alpha 1 and beta 1 subunits (sGC). Cells are preincubated with40 microM 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), an sGCinhibitor, for one h in buffer containing 0.1% bovine serum albumin and3-isobutyl-1-methylxanthine (IBMX). Concentration response curves areprepared for test compounds in DMSO. An intermediate dilution of thecompounds is performed in either buffer containing IBMX or type AB HScontaining IBMX. Diluted compounds are added to cells and they areincubated at room temperature for thirty min. cGMP is measured using aCisBio homogeneous time resolved fluorescence kit and the EC₅₀ iscalculated for each compound.

Representative compounds of the present invention were tested foractivity the above assay. Preferred compounds have an EC₅₀ of <1,000 nMin the above assay and more preferred compounds have an EC₅₀<200 nM. Asexamples, data for representative compounds from Table 1 are shown inTable 2.

TABLE 2 Compound Number EC₅₀ (nM) 1 39 2 11 3 29 4 11 5 9. 6 87 7 32 842 9 59 10 16 11 17 12 26 13 180 14 18 15 28 16 23 17 18 18 8 19 17 2024 21 17 22 14 23 52 24 54 25 16 26 5 27 14 28 13 29 3.5 30 10 31 19 32170 33 97 34 65 35 29 36 27 37 120 38 66 39 17 40 62 41 27 42 24 43 13044 44 45 26 46 38 47 22 48 10 49 54 50 990 51 72 52 170 53 110 54 110 55110 56 820 57 24 58 82 59 31 60 — 61 59 62 24 63 82 64 71 65 56 66 11067 320 68 38 69 61 70 180 71 67 72 17 73 250 74 73 75 23 76 160 77 31 7848 79 33 80 45 81 410 82 8 83 29 84 9 85 22 86 41 87 55 88 28 89 150 9069 91 75 92 20 93 37 94 45 95 54 96 24 97 67 98 270 99 160 100 170 101110 102 110 103 110 104 31 105 17 106 27 107 23 108 24 109 34 110 45 11199 112 110 113 24 114 40 115 68 116 28 117 29 118 39 119 57 120 12 12140 122 23 123 55 124 47 125 27 126 58 127 7.5 128 15 129 17 130 21 131410 132 11 133 27 134 46 135 54 136 81 137 89 138 54 139 8.4 140 15 14117 142 62 143 160 144 460 145 13 146 23 147 450 148 43 149 44 150 91 151130 152 14 153 26 154 28 155 86 156 720 157 25 158 30 159 53 160 110 16114 162 23 163 55 164 32 165 11 166 6.6 167 30 168 580 169 13 170 28 17116 172 50 173 13 174 14 175 40 176 9.7 177 35 178 14 179 59 180 28 18162 182 370 183 980 184 12 185 30 186 16 187 14 188 8.6 189 12 190 23 1913.3 192 10 193 12 194 87 195 4.7 196 13 197 19 198 5.3 199 9 200 20 20112 202 12 203 4.4 204 4.5 205 13 206 7.4 207 9.2 208 20 209 200 210 19211 30 212 36 213 39 214 30 215 37 216 110 217 35 218 62 219 140 220 150221 210 222 5.4 223 8.5 224 79 225 10 226 12 227 13 228 14 229 3.9 23013 231 4.6 232 9.5 233 11 234 13 235 20 236 28 237 4.9 238 5.1 239 6.5240 7.9 241 8 242 11 243 16 244 23 245 280 246 6.5 247 8.6 248 4.2 2494.6 250 44 251 7 252 10 253 13 254 25 255 9.5 256 14 257 14 258 15

Assessment of Solubility

Solubility is measured by the following method.

1. Sample Preparation:

100 uL, 10 mM DMSO stock solution of each compound is prepared in a 96well plate format. The experiment is done in single determination at 3pH values (2.2, 4.5 and 6.8). For each pH and one reference, 40 uL ofeach compound is needed.

Buffer Preparation:

McIlvaine pH 2.2: To 2.076 g citric acid monohydrate and 0.043 gNa₂HPO₄×₂H₂O add 100 ml deionized water

McIlvaine pH 4.5: To 1.166 g citric acid monohydrate and 1.585 gNa₂HPO₄×₂H₂O add 100 ml deionized water

McIlvaine pH 6.8: To 0.476 g citric acid monohydrate and 2.753 gNa₂HPO₄×₂H₂O add 100 ml deionized water

With a suitable liquid handling device (Multipette® or a liquid handler)390 uL of each buffer solution and 10 uL of compound is added to eachwell of a 96 deep well plate. The plates are covered firmly and shakenfor 24 h on an over head shaker (at 54 RPM) at room temperature. TheDMSO content in the final buffer is 2.5% v/v.

After 24 h the plates are centrifuged to remove droplets on the lidbefore opening (for ˜5 min at 2500 RPM).

The filtration is done under vacuum with Millipore 96 well filter plate.Filtrate is collected in a deep well plate and transferred to a suitableplate for UPLC analysis.

The reference plate is prepared by adding 10 uL of compound to 390 uL of50:50 acetonitrile/water in a 96 deep well plate and transferred to asuitable plate for UPLC analysis. Wells are checked visually forprecipitation, any presence noted under comments in reported results.

2. Sample Measurement

The samples are measured with UPLC-UV using the chromatographic methoddescribed below.

stationary phase Waters ACQUITY UPLC ® BEH C18 1.7 μm 2.5 × 50 mm mobilephase solvent A 0.1% formic acid (pH 3) solvent B acetonitrile with 0.1%formic acid Gradient   0 min 5% B 1.0 min 95% B  1.3 min 95% B  1.4 min5% B 1.7 min 5% B column temperature 40° C. Flow 0.8 mL/minduration/cycle time 1.7 min/2.7 min injection volume 2 μL sampletemperature 20° C. PDA detection Enable 3D data wavelength 254 nmsampling rate 40 points/sec resolution 4.8 nm

Waters Empower®2 software is used for generating Sample Sets (accordingto the plate layout), Sample Set Methods and Instrument Methods.

One Sample Set comprises the methods for three 96 well plates (onereference plate and two sample plates, and includes one Sample SetMethod and one Instrument Method).

3. Data Processing and Analysis

The UV chromatograms collected at 254 nm are integrated and processed.

It is assumed that the compound is completely dissolved in the referencesolution (50:50 acetonitrile/water)

Solubility data (μg/mL) for compounds from Table 1 is shown in Table 3below.

TABLE 3 Compound Number (pH 2.2) (pH 4.5) (pH 6.8) 1 95 80 87 2 110 8388 3 96 79 81 4 100 81 83 5 98 76 72 6 90 64 81 7 110 77 91 8 110 82 989 94 70 82 10 94 50 73 11 23 <0.1 80 12 110 90 92 13 100 84 87 14 110 8276 15 110 88 90 16 95 71 81 17 97 62 85 18 110 86 90 19 96 70 75 20 9572 68 21 96 62 60 22 97 68 73 23 99 79 82 24 95 76 76 25 91 38 39 26 10080 80 27 110 88 90 28 110 83 90 29 110 79 78 30 100 81 75 31 110 89 9432 91 73 78 33 93 73 75 34 82 65 68 35 93 73 78 36 91 72 74 37 92 74 7838 110 94 88 39 93 44 81 40 99 81 85 41 96 75 80 42 93 75 78 43 95 79 8244 100 85 88 45 82 61 73 46 100 82 86 47 87 69 79 48 100 82 86 49 92 6958 50 120 79 75 51 110 83 93 52 83 58 73 53 84 65 70 54 100 78 75 55 9848 49 56 87 66 77 57 95 47 51 58 111 85 89 59 — — — 60 117 96 100 61 130110 99 62 110 88 91 63 110 90 92 64 100 66 66 65 110 84 74 66 63 54 5567 90 76 78 68 85 71 74 69 91 77 80 70 86 57 64 71 94 75 78 72 44 46 6773 86 67 71 74 110 83 95 75 120 93 90 76 100 86 89 77 96 83 87 78 100 8689 79 100 87 89 80 110 94 95 81 100 84 79 82 120 100 97 83 110 88 95 84110 86 89 85 120 96 110 86 110 90 91 87 110 87 90 88 90 63 75 89 130 9281 90 100 81 81 91 100 81 81 92 110 93 96 93 98 77 81 94 91 68 73 95 10080 84 96 93 67 75 97 91 72 77 98 150 110 99 99 150 120 110 100 110 88 97101 90 73 74 102 99 81 82 103 96 78 81 104 110 93 97 105 93 72 75 106 8869 73 107 73 54 58 108 81 61 65 109 88 33 36 110 130 96 120 111 87 69 75112 110 78 94 113 94 80 84 114 120 99 100 115 89 71 43 116 — — — 117 10282 85 118 110 84 92 119 110 89 97 120 110 94 97 121 110 90 93 122 100 8682 123 100 76 73 124 100 8.6 44 125 110 76 78 126 96 74 78 127 130 100110 128 93 77 78 129 95 79 79 130 130 100 110 131 130 97 110 132 130 110110 133 120 99 100 134 110 94 100 135 110 97 100 136 120 100 110 137 11098 110 138 — — — 139 130 110 120 140 140 120 120 141 130 110 110 142 12087 93 143 160 150 160 144 110 89 93 145 110 92 94 146 100 88 79 147 1.23.1 75 148 110 100 94 149 110 78 81 150 100 67 78 151 110 98 85 152 9774 74 153 87 67 65 154 85 36 57 155 60 66 73 156 — — — 157 94 70 62 15864 43 41 159 86 55 51 160 <0.1 0.93 73 161 110 91 97 162 100 83 82 163110 75 73 164 100 72 93 165 120 58 39 166 110 51 64 167 2.1 5.9 83 168110 90 88 169 120 100 97 170 120 96 95 171 120 99 98 172 110 87 85 173130 98 97 174 99 71 91 175 110 80 85 176 100 77 43 177 110 58 86 178 10072 86 179 43 92 93 180 100 79 76 181 110 87 88 182 110 81 81 183 110 8287 184 89 76 76 185 100 83 82 186 110 83 99 187 100 82 83 188 89 77 73189 89 73 75 190 100 83 87 191 100 85 80 192 — — — 193 100 80 73 1940.68 2.5 78 195 110 83 80 196 89 77 85 197 110 83 79 198 120 100 93 199120 96 92 200 100 73 73 201 87 68 66 202 92 73 70 203 81 70 72 204 82 7273 205 99 73 81 206 90 71 76 207 82 68 73 208 82 47 57 209 110 81 84 210110 87 87 211 95 82 78 212 92 79 75 213 85 66 72 214 81 64 69 215 86 7076 216 — — — 217 97 73 69 218 120 85 75 219 110 76 74 220 100 77 86 221100 72 94 222 85 71 73 223 81 68 69 224 110 78 13 225 95 78 81 226 98 8386 227 90 73 77 228 96 78 81 229 100 81 73 230 100 84 72 231 120 92 87232 93 74 63 233 98 73 86 234 120 97 91 235 100 83 88 236 110 96 83 23794 55 52 238 77 55 52 239 91 71 72 240 92 69 67 241 100 81 84 242 110 7978 243 100 82 81 244 120 99 98 245 100 79 92 246 — — — 247 90 75 71 24894 75 74 249 94 67 93 250 110 81 86 251 100 72 77 252 94 73 62 253 10075 81 254 100 64 80 255 — — — 256 — — — 257 — — — 258 — — —

Assessment of Metabolic Stability

Objective

The 5 time point, high-throughput human liver microsome (HLM) metabolicstability assay is designed to determine in vitro compound metabolism.Compounds are incubated with HLMs at a concentration of 1 uM, at 37° C.,for a total of 60 min. The percent of compound remaining at 5, 15, 30,and 60 min is used to calculate the t½ (min), CL_(int) (mL/min/kg),CL_(h) (mL/min/kg), and % Q_(h). The assay is based on a 96-well formatand can accommodate up to 92 compounds per plate (n=1).

Incubation

Using the 96-well multi-channel head, the Biomek FX, equipped with aPeltier heating block/shaker, is programmed to accomplish the followingsteps:

-   -   1. Pipette 175 uL of 1.15 mg/mL microsomes into each of the 96        conical inserts (Analytical Sales and Products, catalog number        96PL05) that fit into the plate of the Peltier heating        block/shaker (the incubation plate)    -   2. Add 5 uL of compounds from the assay plate to the microsomes        and shake the mixture at 600 rpm at 42.1° C. for 10 min (a        setting of 42.1° C. on the Peltier is required for the samples        to incubate at 37° C.)    -   3. After 10 min, prompt the user to add the NADPH plate to the        deck and add 20 uL from the NADPH plate to the incubation plate        to start the reaction    -   4. Add 215 uL of 100%, cold acetonitrile containing an internal        standard(s) to a 0 minute, 5 minute, 15 minute, 30 minute, and        60 minute “quench” plate    -   5. At 0 min 5 min, 15 min, 30 min, and 60 min into the        incubation, aspirate 12 uL from the incubation mixture and add        it to the quench solution to stop the reaction    -   6. Add 185 uL HPLC grade water to each well of the 0, 5, 15, 30        and 60 minute quench plates to dilute compounds to the        appropriate concentration for the mass spectrometer

After all time points are collected, the quench plates are sealed with96-well pierceable plate mats or heat sealing foil and centrifuged at3000 rpm for 15 min to pellet the microsomes.

Analysis

The plates are analyzed using LC/MS/MS with electron spray ionization(ESI) and the previously determined MRM transitions. The LC methodincludes the following parameters:

Injection volume: 5 uL

Mobile Phases: 0.1% Formic Acid in Water (A) and 0.1%

Formic Acid in Acetonitrile (B) (HPLC grade)

Left and Right Temperature: 35° C.

Run Time: 4.0 min

Column: Thermo Scientific, Aquasil C18, 50×2.1 mm, 5μ, part number77505-052130, or equivalent

LC Pump Gradient:

Total Time (min) Flow Rate (uL/min) % A % B 0 500 90.0 10.0 0.5 500 90.010.0 1.5 500 1.0 99.0 2.5 500 1.0 99.0 3.3 500 90.0 10.0 4.0 500 90.010.0

If peak shape is poor and cannot be integrated properly, the followingLC method can be used:

Injection volume: 5 uL

Mobile Phases: 2.5 mM Ammonium Bicarbonate (A) and 100% Acetonitrile (B)(HPLC grade)

Aqueous Wash: 90% Water, 10% Acetonitrile (HPLC grade)

Organic Wash: 90% Acetonitrile, 10% Water (HPLC grade)

Left and Right Temperature: 35° C.

Run Time: 4.5 min

Column: Phenomex Luna 3 u C18(2) 100 A, 50×2.00 mm

LC Pump Gradient:

Total Time (min) Flow Rate (uL/min) % A % B 0 500 90.0 10.0 0.5 500 90.010.0 1.5 500 1.0 99.0 2.5 500 1.0 99.0 3.30 500 90.0 10.0 4.50 500 90.010.0

Using an Excel template in Activitybase, the peak areas corresponding to5, 15, 30 and 60 min are compared to the peak area at 0 min to calculatethe percent of remaining compound using the following equation:Percent compound remaining=(AUC at Time t min/AUC at Time 0 min)×100where t=0, 5, 15, 30 or 60 min.

Time (min) is plotted against the natural logarithm (Ln) of the percentcompound remaining to determine the slope. The slope is used tocalculate t½ (min) using the equation, t½=0.693/slope.

Clint, Intrinsic Clearance0.693/t½* Avg liver wt in g/avg body wt in kg*f(u)/protein concentrationin incubation in mg/mL*mg microsomal protein/g liver0.693/t½*26 g/kg*1/1.0 mg/mL*45 mg/gClh, Hepatic ClearanceHepatic flow*f(u)*Clint/(hepatic flow+f(u)*Clint)Qh, % Hepatic Blood Flow(Clh/Hepatic flow)*100

Metabolic stability data (% Qh) for compounds from Table 1 is shown inTable 4 below. Preferred compounds have % Qh values of less than 24.

TABLE 4 Compound Number. HLM (% Qh) 1 <24 2 <24 3 <24 4 <24 5 <24 6 <247 <24 8 <24 9 <24 10 30 11 47 12 <24 13 <24 14 31 15 <24 16 <24 17 31 18<24 19 29 20 38 21 <24 22 33 23 <24 24 <24 25 29 26 29 27 <24 28 <24 2928 30 <24 31 <24 32 <24 33 <24 34 <24 35 <24 36 <24 37 <24 38 <24 39 <2440 <24 41 <24 42 <24 43 26 44 <24 45 <24 46 <24 47 <24 48 <24 49 48 5040 51 <24 52 <24 53 <24 54 <24 55 <24 56 <24 57 <24 58 <24 59 <24 60 <2461 <24 62 <24 63 <24 64 <24 65 <24 66 <24 67 <24 68 <24 69 <24 70 <24 71<24 72 47 73 36 74 <24 75 31 76 <24 77 <24 78 <24 79 <24 80 <24 81 <2482 <24 83 <24 84 <24 85 <24 86 <24 87 <24 88 <24 89 76 90 <24 91 <24 92<24 93 <24 94 <24 95 <24 96 30 97 <24 98 31 99 <24 100 31 101 <24 102<24 103 25 104 26 105 <24 106 <24 107 <24 108 <24 109 <24 110 <24 111<24 112 <24 113 <24 114 <24 115 25 116 <24 117 25 118 <24 119 <24 120<24 121 <24 122 <24 123 <24 124 <24 125 <24 126 <24 127 <24 128 <24 129<24 130 25 131 28 132 <24 133 <24 134 32 135 29 136 <24 215 <24 216 <24217 89 218 89 219 89 220 <24 221 <24 222 <24 223 <24 224 <24 225 <24 22652 227 25 228 44 229 34 230 <24 231 <24 232 <24 233 26 234 <24 235 29236 <24 237 <24 238 <24 239 25 240 <24 241 <24 242 <24 243 <24 244 <24245 <24 246 <24 247 <24 248 <24 249 <24 250 <24 251 <24 252 <24 253 <24254 <24 255 <24 256 <24 257 <24 258 <24 137 <24 138 68 139 <24 140 <24141 <24 142 <24 143 <24 144 <24 145 <24 146 <24 147 <24 148 <24 149 <24150 <24 151 <24 152 <24 153 <24 154 <24 155 <24 156 <24 157 31 158 <24159 <24 160 44 161 <24 162 26 163 <24 164 <24 165 <24 166 27 167 <24 168<24 169 <24 170 <24 171 <24 172 <24 173 <24 174 <24 175 31 176 28 177<24 178 <24 179 <24 180 <24 181 <24 182 <24 183 <24 184 <24 185 <24 186<24 187 <24 188 <24 189 26 190 43 191 <24 192 <24 193 <24 194 <24 195<24 196 <24 197 <24 198 <24 199 <24 200 40 201 <24 202 <24 203 <24 204<24 205 <24 206 <24 207 <24 208 <24 209 <24 210 <24 211 <24 212 <24 213<24 214 <24

Methods of Therapeutic Use

The compounds disclosed herein effectively activate soluble guanylatecyclase. The activation or potentiation of soluble guanylate cyclase isan attractive means for preventing and treating a variety of diseases orconditions associated with deficient sGC activation. Thus, in oneembodiment of the invention, there are provided methods of treatingdiseases that can be alleviated by sGC activation or potentiation. Theseinclude:

Cardiovascular and related diseases including hypertension,atherosclerosis, peripheral artery disease, restenosis, stroke, heartfailure, coronary vasospasm, cerebral vasospasm, ischemia/reperfusioninjury, thromboembolic pulmonary hypertension, pulmonary arterialhypertension, stable and unstable angina and thromboembolic disorders;Inflammatory diseases including psoriasis, multiple sclerosis,arthritis, asthma, and chronic obstructive pulmonary disease;Hepatic fibrotic disorders including but not limited to cirrhosis of anyetiology or fibrosis of specific areas of the liver such as periportalfibrosis which may be caused by immunologic injury, hemodynamic effectsand/or other causes;Renal fibrotic disorders including but not limited toglomerulosclerosis, focal glomerulosclerosis, mesangial fibrosis,interstitial fibrosis due to immunologic injury, hemodynamic effects,diabetes (types I and 2), diabetic nephropathy, IgA nephropathy, lupusnephropathy, membranous nephropathy, hypertension, hemolytic uremicsyndrome, multiple glomerulonephritides, interstitial nephritis,tubulointerstitial nephritis again of immunologic and non-immunologiccauses;Pulmonary fibrotic disorders, both diffuse and localized, due toimmunologic and non-immunologic causes, including but not limited toidiopathic pulmonary fibrosis, pulmonary fibrosis due to exposure totoxins, chemicals, drugs, and cystic fibrosis;Cardiac fibrotic disorders due to immunologic and non-immunologic causesincluding ischemic heart disease (coronary artery disease) and transientand/or sustained decreased blood flow in one or more coronary vesselsincluding possibly related to interventions on coronary arteries orveins, associated with cardiac surgery and/or the use of cardiopulmonarybypass procedures and myocarditis due to viral and non-viral causes, aswell as immunologically related myocardial injury potentially due tocross-reactivity to other antigens to which the human body is exposed;Other diseases mediated at least partially by diminished or decreasedsoluble guanylate cyclase activity, such as renal disease, diabetes,urologic disorders including overactive bladder, benign prostatichyperplasia, and erectile dysfunction, and neurological disordersincluding Alzheimer's disease, Parkinson's disease and neuropathic pain.

These disorders have been well characterized in man, but also exist witha similar etiology in other mammals, and can be treated bypharmaceutical compositions of the present invention.

For therapeutic use, the compounds of the invention may be administeredvia a pharmaceutical composition in any conventional pharmaceuticaldosage form in any conventional manner.

Conventional dosage forms typically include a pharmaceuticallyacceptable carrier suitable to the particular dosage form selected.Routes of administration include, but are not limited to, intravenously,intramuscularly, subcutaneously, intrasynovially, by infusion,sublingually, transdermally, orally, topically or by inhalation. Thepreferred modes of administration are oral and intravenous.

The compounds of this invention may be administered alone or incombination with adjuvants that enhance stability of the inhibitors,facilitate administration of pharmaceutical compositions containing themin certain embodiments, provide increased dissolution or dispersion,increase inhibitory activity, provide adjunct therapy, and the like,including other active ingredients. In one embodiment, for example,multiple compounds of the present invention can be administered.Advantageously, such combination therapies utilize lower dosages of theconventional therapeutics, thus avoiding possible toxicity and adverseside effects incurred when those agents are used as monotherapies.Compounds of the invention may be physically combined with theconventional therapeutics or other adjuvants into a singlepharmaceutical composition. Advantageously, the compounds may then beadministered together in a single dosage form. In some embodiments, thepharmaceutical compositions comprising such combinations of compoundscontain at least about 5%, but more preferably at least about 20%, of acompound of formula (I) (w/w) or a combination thereof. The optimumpercentage (w/w) of a compound of the invention may vary and is withinthe purview of those skilled in the art. Alternatively, the compounds ofthe present invention and the conventional therapeutics or otheradjuvants may be administered separately (either serially or inparallel). Separate dosing allows for greater flexibility in the dosingregimen.

As mentioned above, dosage forms of the compounds of this invention mayinclude pharmaceutically acceptable carriers and adjuvants known tothose of ordinary skill in the art and suitable to the dosage form.These carriers and adjuvants include, for example, ion exchangers,alumina, aluminum stearate, lecithin, serum proteins, buffer substances,water, salts or electrolytes and cellulose-based substances. Preferreddosage forms include tablet, capsule, caplet, liquid, solution,suspension, emulsion, lozenges, syrup, reconstitutable powder, granule,suppository and transdermal patch. Methods for preparing such dosageforms are known (see, for example, H. C. Ansel and N. G. Popovish,Pharmaceutical Dosage Forms and Drug Delivery Systems, 5th ed., Lea andFebiger (1990)). Dosage levels and requirements for the compounds of thepresent invention may be selected by those of ordinary skill in the artfrom available methods and techniques suitable for a particular patient.In some embodiments, dosage levels range from about 1-1000 mg/dose for a70 kg patient. Although one dose per day may be sufficient, up to 5doses per day may be given. For oral doses, up to 2000 mg/day may berequired. As the skilled artisan will appreciate, lower or higher dosesmay be required depending on particular factors. For instance, specificdosage and treatment regimens will depend on factors such as thepatient's general health profile, the severity and course of thepatient's disorder or disposition thereto, and the judgment of thetreating physician.

What is claimed is:
 1. A compound of the formula I

wherein: A is a 5-7 membered saturated heterocyclyl group containing onenitrogen and optionally one oxygen, wherein one carbon of saidheterocyclyl group is optionally substituted with one or two groupsselected from C₁₋₃alkyl and oxo; R¹ is C₁₋₄ alkyl optionally substitutedwith a methoxy group; R² is selected from H, F, Cl, C₁₋₃alkyl, —CN, —OMeand —CF₃; R³ is selected from H and —CH₃; R⁴ is selected from H, F, —CH₃and —OMe; R⁵ is selected from H, Cl, —CH₃, —CH₂CH₃, —CF₃, F, and —OMe;R⁶ is bonded to the nitrogen on A and is selected from H, C₁₋₆alkyl,—(CH₂)_(n)C₃₋₆cycloalkyl, —C(O)C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl,—(CH₂)_(n) aryl —(CH₂)_(n) heteroaryl, —SO₂aryl, SO₂C₁₋₆alkyl whereinsaid C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl, —(CH₂)_(n) cycloalkyl,—(CH₂)_(n) aryl and —(CH₂)_(n) heteroaryl are optionally substitutedwith one to four groups independently selected from C₁₋₃alkyl, halogen,C₁₋₃alkoxy, —CF₃, —OH, oxo, —(CH₂)₁₋₃O(CH₂)₂₋₃OH, and —SO₂CH₃; R⁷ isselected from H, —CH₃, —CH₂CH₃, —CF₃, F, and —CN; n is 0, 1 or 2 or asalt thereof.
 2. The compound according to claim 1, wherein: A is a 5-7membered saturated heterocyclyl group containing one nitrogen, whereinone carbon of said heterocyclyl group is optionally substituted with oneor two C₁₋₃alkyl groups; R¹ is C₁₋₃alkyl; R⁴ is selected from H and F;R⁵ is selected from H, Cl and —CH₃; R⁶ is bonded to the nitrogen on Aand is selected from H, C₁₋₆alkyl, —(CH₂)_(n)C₃₋₆cycloalkyl,—C(O)C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl, —(CH₂)_(n) aryl and —(CH₂)_(n)heteroaryl, wherein said C₁₋₆alkyl, —(CH₂)_(n) heterocyclyl, —(CH₂)_(n)cycloalkyl, —(CH₂)_(n) aryl and —(CH₂)_(n) heteroaryl are optionallysubstituted with one to four groups independently selected fromC₁₋₃alkyl, halogen, C₁₋₃alkoxy, —CF₃, —OH and —SO₂CH₃; and R⁷ is H; or asalt thereof.
 3. The compound according to claim 1, wherein: R¹ ismethyl, ethyl or isopropyl; and the group

 is selected from:

or a salt thereof.
 4. The compound according to claim 1, wherein: R² isselected from —CH₃, F, Cl, and —CF₃; and R⁶ is selected from H,C₁₋₆alkyl, —(CH₂)_(n)C₃₋₆cycloalkyl, —C(O)C₁₋₆alkyl and —(CH₂)_(n)heterocyclyl, wherein said C₁₋₆alkyl, —(CH₂)_(n) cycloalkyl and—(CH₂)_(n) heterocyclyl are optionally substituted with one to fourgroups independently selected from C₁₋₃alkyl, halogen, C₁₋₃alkoxy, —CF₃,—OH and —SO₂CH₃; or a salt thereof.
 5. The compound according to claim1, wherein each heterocyclyl referred to in R⁶ is selected fromoxetanyl, tetrahydrofuranyl, tetrahydropyranyl,2-oxabicyclo[3.2.0]heptanyl, [1,4]dioxanyl, 8-oxabicyclo [3.2.1]octanyl,1-oxaspiro[4.5]decanyl and pyrrolidin-2-one; each heteroaryl referred toin R⁶ is selected from imidazolyl, isoxazolyl, pyrazinyl, pyrazolyl,pyridinyl, pyrimidinyl, thiazolyl and 4,5,6,7-tetrahydrobenzothiazolyl;and each aryl referred to in R⁶ is phenyl; or a salt thereof.
 6. Thecompound according to claim 1, wherein: R⁶ is —(CH₂)_(n) heterocyclyl,wherein said heterocyclyl is selected from oxetanyl, tetrahydrofuranyl,tetrahydropyranyl, 2-oxabicyclo[3.2.0]heptanyl, [1,4]dioxanyl,8-oxabicyclo[3.2.1]octanyl and 1-oxaspiro[4.5]decanyl; or a saltthereof.
 7. The compound according to claim 1, wherein: R² is —CH₃; R³is H; R⁴ is H or —CH₃; R⁵ is H, or —CH₃; R⁷ is in the position para toR⁵ and is H, —CH₃ or —CH₂CH₃; or a salt thereof.
 8. The compoundaccording to claim 1, wherein: the group

or a salt thereof.
 9. The compound according to claim 1, wherein: R³ isH; and R⁴ is H; or a salt thereof.
 10. The compound according to claim 1selected from the group consisting of Cpd No. Structure 1

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and the pharmaceutically acceptable salts thereof.
 11. The compoundaccording to claim 10 selected from the group consisting of compoundnumbers 1, 2, 3, 4, 5, 7, 8, 9, 12, 15, 16, 18, 21, 27, 28, 30, 31, 35,36, 39, 41, 42, 44, 45, 46, 47, 48, 57, 59, 62, 68, 77, 78, 79, 80, 82,83, 84, 85, 86, 88, 92, 93, and 94 and the pharmaceutically acceptablesalts thereof.
 12. The compound according to claim 10 selected from thegroup consisting of compound numbers 95, 97, 100, 101, 102, 103, 104,105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118,119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132,136, 137, 139, 140, 141, 142, 145, 146, 152, 153, 154, 155, 157, 158,159, 161, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172, 173, 174,175, 176, 177, 178, 179, 180, 181, 184, 185, 186, 187, 188, 189, 191,193, 194, 195, 196, 197, 198, 199, 201, 202, 203, 204, 205, 206, 207,208, 210, 211, 212, 213, 214, 215, 216, 220, 222, 223, 224, 225, 227,229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242,243, 244, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257 andthe pharmaceutically acceptable salts thereof.
 13. A pharmaceuticalcomposition comprising a compound according to claim 1 and apharmaceutically acceptable excipient or carrier.
 14. A method oftreating a disease or disorder that can be alleviated by sGC activationor potentiation, wherein the disease or disorder is selected fromhepatic fibrotic disorder, renal fibrotic disorder, pulmonary fibroticdisorder, cardiac fibrotic disorder, overactive bladder, benignprostatic hyperplasia, erectile dysfunction, Parkinson's disease,neuropathic pain and diabetic nephropathy, comprising administering atherapeutically effective amount of a compound according to claim 1 topatient in need thereof.
 15. The method according to claim 14 whereinthe disease is diabetic nephropathy.
 16. A compound, wherein thecompound is

or a pharmaceutically acceptable salt thereof.
 17. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 18. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 19. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 20. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 21. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 22. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 23. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 24. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 25. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 26. A pharmaceuticalcomposition comprising a compound according to claim 16 and apharmaceutically acceptable excipient or carrier.
 27. A pharmaceuticalcomposition comprising a compound according to claim 17 and apharmaceutically acceptable excipient or carrier.
 28. A pharmaceuticalcomposition comprising a compound according to claim 18 and apharmaceutically acceptable excipient or carrier.
 29. A pharmaceuticalcomposition comprising a compound according to claim 19 and apharmaceutically acceptable excipient or carrier.
 30. A pharmaceuticalcomposition comprising a compound according to claim 20 and apharmaceutically acceptable excipient or carrier.
 31. A pharmaceuticalcomposition comprising a compound according to claim 21 and apharmaceutically acceptable excipient or carrier.
 32. A pharmaceuticalcomposition comprising a compound according to claim 22 and apharmaceutically acceptable excipient or carrier.
 33. A pharmaceuticalcomposition comprising a compound according to claim 23 and apharmaceutically acceptable excipient or carrier.
 34. A pharmaceuticalcomposition comprising a compound according to claim 24 and apharmaceutically acceptable excipient or carrier.
 35. A pharmaceuticalcomposition comprising a compound according to claim 25 and apharmaceutically acceptable excipient or carrier.
 36. A compound,wherein the compound is

or a pharmaceutically acceptable salt thereof.
 37. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 38. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 39. A compound, whereinthe compound is

or a pharmaceutically acceptable salt thereof.
 40. A pharmaceuticalcomposition comprising a compound according to claim 36 and apharmaceutically acceptable excipient or carrier.
 41. A pharmaceuticalcomposition comprising a compound according to claim 37 and apharmaceutically acceptable excipient or carrier.
 42. A pharmaceuticalcomposition comprising a compound according to claim 38 and apharmaceutically acceptable excipient or carrier.
 43. A pharmaceuticalcomposition comprising a compound according to claim 39 and apharmaceutically acceptable excipient or carrier.